Piperidines
Organic heterocyclic compounds that consist of a six-membered ring containing five carbon atoms and one nitrogen atom that forms an amine functional group.
Quantity
- (229)
- (1)
- (24)
- (10)
- (40)
- (5)
- (5)
- (1)
- (1)
- (1)
- (6)
- (131)
- (7)
- (5)
- (4)
- (4)
- (52)
- (236)
- (5)
- (5)
- (3)
- (9)
- (13)
- (5)
- (1)
- (1)
Molecular Weight (g/mol)
- (4)
- (4)
- (3)
- (1)
- (1)
- (14)
- (2)
- (1)
- (1)
- (1)
- (1)
- (6)
- (8)
- (2)
- (2)
- (15)
- (3)
- (1)
- (1)
- (11)
- (5)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (2)
- (3)
- (5)
- (2)
- (1)
- (11)
- (8)
- (4)
- (1)
- (1)
- (2)
- (4)
- (4)
- (9)
- (7)
- (2)
- (1)
- (1)
- (2)
- (6)
- (3)
- (5)
- (1)
- (2)
- (2)
- (1)
- (3)
- (2)
- (1)
- (2)
- (3)
- (2)
- (3)
- (5)
- (3)
- (6)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (3)
- (2)
- (2)
- (1)
- (7)
- (1)
- (8)
- (2)
- (2)
- (1)
- (2)
- (16)
- (3)
- (14)
- (1)
- (1)
- (4)
- (3)
- (1)
- (3)
- (1)
- (1)
- (14)
- (1)
- (2)
- (10)
- (1)
- (5)
- (2)
- (2)
- (1)
- (10)
- (8)
- (6)
- (1)
- (1)
- (9)
- (3)
- (3)
- (2)
- (2)
- (1)
- (2)
- (3)
- (3)
- (1)
- (1)
- (1)
- (3)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (2)
- (6)
- (2)
- (11)
- (8)
- (1)
- (7)
- (6)
- (5)
- (2)
- (4)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (2)
- (1)
- (2)
- (4)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (12)
- (11)
- (6)
- (2)
- (2)
- (1)
- (1)
- (2)
- (3)
- (2)
- (1)
- (3)
- (3)
- (1)
- (1)
- (1)
- (4)
- (8)
- (1)
- (2)
- (2)
- (4)
- (2)
- (1)
- (2)
- (1)
- (9)
- (4)
- (4)
- (2)
- (1)
- (1)
- (8)
- (1)
- (2)
- (1)
- (1)
- (5)
- (2)
- (2)
- (2)
- (1)
- (5)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (2)
- (3)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (9)
- (8)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (6)
- (1)
- (3)
- (3)
- (5)
- (1)
- (3)
- (2)
- (2)
- (1)
- (3)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (3)
- (1)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (1)
- (3)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (4)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (8)
Percent Purity
- (1)
- (2)
- (3)
- (5)
- (7)
- (4)
- (15)
- (2)
- (15)
- (3)
- (4)
- (4)
- (2)
- (4)
- (2)
- (2)
- (1)
- (20)
- (49)
- (68)
- (4)
- (4)
- (17)
- (3)
- (19)
- (2)
- (1)
- (4)
- (9)
- (2)
- (12)
- (42)
- (1)
- (1)
- (9)
- (246)
- (95)
- (1)
- (47)
- (3)
- (1)
Physical Form
- (2)
- (3)
- (13)
- (161)
- (2)
- (7)
- (2)
- (3)
- (2)
- (2)
- (5)
- (2)
- (2)
- (116)
- (1)
- (1)
- (1)
- (2)
- (26)
- (45)
- (3)
Boiling Point
- (3)
- (2)
- (3)
- (2)
- (6)
- (2)
- (1)
- (3)
- (3)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (3)
- (1)
- (4)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (3)
- (3)
- (2)
- (3)
- (2)
- (2)
- (3)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (4)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (3)
- (2)
- (2)
- (2)
- (1)
- (1)
- (6)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
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1,981
eMolecules PIPERIDINE-4-CARBOXYLIC AC 25G
5000225146 PIPERIDINE-4-CARBOXYLIC AC 25G
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1,982
eMolecules EMOLECULES INC
5000470948 TERT-BUTYL PIPERIDINE-4-CA 10G
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1,983
eMolecules EMOLECULES INC
5000471043 4-AMINO-1-BOC-PIPERIDINE-4- 1G
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1,984
eMolecules EMOLECULES INC
5000471508 TERT-BUTYL PIPERIDINE-4-CAR 1G
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1,985
eMolecules EMOLECULES INC
5000471858 TERT-BUTYL PIPERIDINE-4-CAR 1G
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1,986
eMolecules EMOLECULES INC
5000471859 TERT-BUTYL PIPERIDINE-4-CAR 5G
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1,987
eMolecules EMOLECULES INC
5000473343 R-N-FMOC-PIPERIDINE-2-CAR 5G
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1,988
eMolecules EMOLECULES INC
5000483439 TERT-BUTYL PIPERIDINE-4-CAR 1G
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1,989
Chemscene CHEMSCENE
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5000576843 ETHYL N-BOC-PIPERIDINE-4-C 1KG
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1,990
eMolecules EMOLECULES INC
NC3962223 S-PIPERIDINE-2-CARBOXAMIDE
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1,991
Chembridge Corporation 4-(BENZYLOXY)PIPERIDINE
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4-(benzyloxy)piperidine. 76716-51-3 MFCD07186358
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1,992
eMolecules Medchem Express / TAK-960 / 5mg / 446265042 / HY-15160 / / 1137868-52-0 / MFCD22420821 / 561.610 / C27H34F3N7O3
Medchem Express / TAK-960 / 5mg / 446265042 / HY-15160 / / 1137868-52-0 / MFCD22420821 / 561.610 / C27H34F3N7O3
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1,993
Medchemexpress LLC 3-Amino-2,6-piperidinedione | 2353-44-8 | 99.96% | 128.13 | 500 MG
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3-Amino-2,6-piperidinedione is a synthetic intermediate utilized in the design of antitumor compounds. This product is for research use only and is not sold to patients.
- Synthetic intermediate.
- Used in the design of antitumor compounds.
- Purity: 99.96%.
- Available in multiple pack sizes (e.g., 250 mg, 500 mg, 1 g, 5 g, 10 g, 25 g, 50 g).
- Appearance: Solid, off-white to light blue.
- Shipping: Room temperature (continental US).
- Storage: 4°C, protected from light.
- Storage in solvent: -80°C for 6 months; -20°C for 1 month (protected from light).
- For research use only.
- Cited in scientific literature for its use in synthesizing antitumor agents.
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1,994
![Medchemexpress LLC 3-[1-[(3S)-1-prop-2-enoylpyrrolidin-3-yl]oxyisoquinolin-3-yl]-1,4-dihydro-1,2,4-triazol-5-one | 1627603-21-7 | 99.9% | C18H17N5O3 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260119.png-250.jpg)
Medchemexpress LLC 3-[1-[(3S)-1-prop-2-enoylpyrrolidin-3-yl]oxyisoquinolin-3-yl]-1,4-dihydro-1,2,4-triazol-5-one | 1627603-21-7 | 99.9% | C18H17N5O3 | 10MG
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Small and Specialty Supplier Partner
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TAK-020 is a covalent Bruton's tyrosine kinase (BTK) inhibitor developed by Takeda and advanced as a clinical candidate for hematologic malignancies and autoimmune diseases. It irreversibly binds Cys481 in BTK's ATP-binding site and is provided by research suppliers as a characterized small-molecule reagent (CAS 1627603-21-7).
- Covalent inhibitor that targets Cys481 in BTK.
- Selective BTK inhibition supported by preclinical and clinical data.
- Well-characterized small molecule with published analytical reports.
- Available from vendors in mg-scale quantities for research use.
- Typically supplied as high-purity material for in vitro and in vivo studies.
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1,995
eMolecules Combi-Blocks N-Boc-piperidine-4-carboxylic acid 1kg 290684670 AM-1030 98 000 84358-13-4 MFCD00076999 229 276 C11H19NO4
Combi-Blocks N-Boc-piperidine-4-carboxylic acid 1kg 290684670 AM-1030 98 000 84358-13-4 MFCD00076999 229 276 C11H19NO4
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