Pyrrolidines
Organic heterocyclic compounds that consist of a five-membered ring with four carbon atoms and one nitrogen atom that form a cyclic secondary amine.
Quantity
- (1)
- (295)
- (4)
- (2)
- (4)
- (1)
- (28)
- (3)
- (10)
- (54)
- (1)
- (10)
- (51)
- (3)
- (1)
- (3)
- (3)
- (1)
- (1)
- (3)
- (6)
- (1)
- (2)
- (1)
- (8)
- (1)
- (125)
- (2)
- (14)
- (23)
- (11)
- (4)
- (65)
- (1)
- (1)
- (1)
- (2)
- (234)
- (8)
- (6)
- (6)
- (10)
- (5)
- (1)
- (18)
- (39)
- (9)
- (8)
- (2)
- (1)
Molecular Weight (g/mol)
- (1)
- (1)
- (1)
- (4)
- (12)
- (12)
- (3)
- (5)
- (1)
- (10)
- (35)
- (2)
- (13)
- (1)
- (3)
- (6)
- (7)
- (4)
- (1)
- (7)
- (8)
- (3)
- (8)
- (1)
- (1)
- (2)
- (8)
- (4)
- (2)
- (2)
- (12)
- (9)
- (1)
- (4)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (3)
- (2)
- (6)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (3)
- (2)
- (4)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (3)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (5)
- (5)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (10)
- (3)
- (3)
- (4)
- (1)
- (1)
- (1)
- (1)
- (5)
- (2)
- (1)
- (1)
- (3)
- (1)
- (1)
- (7)
- (4)
- (5)
- (1)
- (1)
- (2)
- (1)
- (2)
- (8)
- (2)
- (1)
- (2)
- (2)
- (5)
- (1)
- (2)
- (7)
- (9)
- (1)
- (1)
- (1)
- (5)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (3)
- (1)
- (2)
- (4)
- (1)
- (2)
- (2)
- (4)
- (1)
- (1)
- (3)
- (2)
- (6)
- (6)
- (4)
- (1)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (4)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (2)
- (2)
- (4)
- (1)
- (1)
- (3)
- (6)
- (1)
- (2)
- (1)
- (1)
- (3)
- (14)
- (1)
- (2)
- (1)
- (1)
- (3)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (3)
- (9)
- (2)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (5)
- (1)
- (3)
- (5)
- (1)
- (1)
- (1)
- (1)
- (1)
- (5)
- (2)
- (4)
- (1)
- (1)
- (1)
- (3)
- (4)
- (8)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (11)
- (1)
- (5)
- (1)
- (1)
- (10)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (3)
- (4)
- (3)
- (4)
- (3)
- (1)
- (1)
- (2)
- (5)
- (1)
- (4)
- (1)
- (1)
- (2)
- (2)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (5)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (3)
- (2)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (7)
- (1)
- (3)
- (2)
- (1)
- (1)
- (1)
- (4)
- (3)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (11)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (3)
- (2)
- (1)
- (8)
- (2)
- (4)
- (1)
- (1)
- (1)
- (2)
- (5)
- (2)
- (3)
- (1)
- (2)
- (4)
- (1)
- (2)
- (1)
- (4)
- (1)
- (1)
- (4)
- (2)
- (1)
- (3)
- (1)
- (1)
- (10)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (4)
- (3)
- (8)
- (1)
- (2)
- (1)
- (1)
- (3)
- (4)
- (6)
- (1)
- (1)
- (12)
- (2)
- (2)
Percent Purity
- (2)
- (1)
- (1)
- (2)
- (1)
- (9)
- (2)
- (4)
- (2)
- (1)
- (5)
- (2)
- (4)
- (4)
- (15)
- (2)
- (2)
- (3)
- (2)
- (3)
- (9)
- (1)
- (1)
- (33)
- (74)
- (3)
- (33)
- (20)
- (38)
- (13)
- (13)
- (41)
- (5)
- (1)
- (1)
- (11)
- (1)
- (2)
- (1)
- (2)
- (5)
- (3)
- (2)
- (3)
- (5)
- (3)
- (19)
- (49)
- (16)
- (1)
- (177)
- (8)
- (114)
- (2)
- (2)
- (5)
- (1)
- (66)
- (4)
- (3)
Physical Form
- (3)
- (13)
- (248)
- (6)
- (5)
- (1)
- (2)
- (2)
- (5)
- (3)
- (8)
- (3)
- (137)
- (3)
- (4)
- (2)
- (39)
- (4)
- (2)
- (54)
Boiling Point
- (1)
- (2)
- (1)
- (2)
- (2)
- (8)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (4)
- (2)
- (2)
- (1)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (4)
- (3)
- (2)
- (4)
- (2)
- (1)
- (1)
- (1)
- (5)
- (4)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (3)
- (2)
- (2)
- (1)
- (1)
- (2)
- (4)
- (1)
- (8)
- (1)
- (5)
- (3)
- (4)
- (2)
- (3)
- (1)
- (2)
- (2)
- (5)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (4)
- (2)
- (1)
- (3)
- (1)
- (1)
- (1)
- (4)
- (3)
- (2)
- (2)
- (1)
- (2)
- (4)
- (2)
- (2)
- (2)
- (3)
- (1)
- (1)
- (1)
- (2)
- (3)
- (2)
- (2)
- (3)
- (2)
- (2)
- (3)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (3)
- (2)
- (4)
- (1)
- (2)
- (3)
- (2)
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3,631
Medchemexpress LLC Azido-PEG6-C2-Boc | 406213-76-1 | 99.8% | C19H37N3O8 | 500 MG
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Azido-PEG6-C2-Boc is a PEG-based PROTAC linker used in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group that can participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker
- Used in PROTAC synthesis
- Click chemistry reagent with Azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Allows strain-promoted alkyne-azide cycloaddition (SPAAC)
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3,632
Medchemexpress LLC Azido-PEG9-Boc | 1818294-43-7 | C25H49N3O11 | 100 MG
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Azido-PEG9-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It functions as a click chemistry reagent, containing an Azide group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Alkyne groups. Additionally, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
- Used in the synthesis of PROTACs
- Functions as a click chemistry reagent
- Contains an azide group
- Facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC)
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3,633
Medchemexpress LLC Azido-PEG1-Boc | 1374658-85-1 | 98.0% | C9H17N3O3 | 50 MG
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Azido-PEG1-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is a click chemistry reagent containing an Azide group. It can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups, and also strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Click chemistry reagent
- Contains an azide group
- Enables copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Enables strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Used in the synthesis of PROTACs
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3,634
Medchemexpress LLC Azido-PEG10-Boc | 250MG
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Azido-PEG10-Boc | 250MG
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3,635
eMolecules 2-CHLORO-5-HYDROXYMETHYL 25G
5000158786 2-CHLORO-5-HYDROXYMETHYL 25G
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3,636
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431122 CYANINE5.5 MALEIMIDE 1MG
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3,637
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431283 AF 488 MALEIMIDE 1MG
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3,638
eMolecules 1-BOC-3-AMINOMETHYLAZETIDIN 1G
5000216984 1-BOC-3-AMINOMETHYLAZETIDIN 1G
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3,639
eMolecules 1-TERT-BUTOXYCARBONYL- 0.25G
5000216997 1-TERT-BUTOXYCARBONYL- 0.25G
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3,640
Medchemexpress LLC tert-butoxycarbonyl methionine | 93000-03-4 | MFCD00190811 | 95.0% | 249.33 g/mol | C10H19NO4S | 100 G
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(tert-Butoxycarbonyl)methionine is the N-tert-butoxycarbonyl (Boc) protected derivative of the amino acid methionine. It is supplied as a white to off-white solid and is used as an N-protected building block in peptide synthesis and other organic synthesis applications where temporary protection of the amino terminus is required.
- Used as an N-protected amino acid building block for peptide synthesis.
- Provides tert-butoxycarbonyl (Boc) protection of the amino terminus.
- Supplied as a white to off-white solid for ease of handling and storage.
- High purity suitable for synthetic applications (listed purity 95.0%).
- Characterized by formula C10H19NO4S and molecular weight 249.33 g/mol.
- Documentation available: certificate of analysis and safety data sheet.
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3,641
Medchemexpress LLC Tert-butoxycarbonyl-L-valyl-L-valine | 69209-73-0 | 97.0% | 316.39 g/mol | C15H28N2O5 | 10 G
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(tert-Butoxycarbonyl)-L-valyl-L-valine is a Boc-protected dipeptide derived from two valine residues, used as a building block in peptide synthesis and related biochemical research applications.
- Boc-protected L-valyl-L-valine dipeptide for peptide synthesis.
- White to off-white powder; molecular weight 316.39 g/mol.
- Chemical formula C15H28N2O5; CAS number 69209-73-0.
- Purity 97.0%.
- Typical package: 10 G; powder storage -20°C (3 years), 4°C (2 years).
- In solvent storage -80°C (6 months), -20°C (1 month).
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3,642
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701762 BR-PEG3-C2-BOC 1G
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3,643
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701945 Z-LAFUTIDINE 1G
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3,644
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701231 Z-VRPR-FMK 10MG
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3,645
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000701535 Z-VRPR-FMK 500UG
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