Phenylcarbamic acid esters
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Filtered Search Results
Medchemexpress LLC 4-IODOANILINE 98 25G
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4-IODOANILINE 98 25G
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Medchemexpress LLC HUMAN CD8 T CELLS N 2ML
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HUMAN CD8 T CELLS N 2ML
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Medchemexpress LLC REGORAFENIB N-OXYDE 1 mg
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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REGORAFENIB N-OXYDE 1MG
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Medchemexpress LLC 4-IODOANILINE 98 100G
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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4-IODOANILINE 98 100G
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eMolecules 273206-92-1 | EXO-6-AMINO-3-BOC-3-AZABICYCLO[3.1.0]HEXANE | AstaTech | MFCD09832898 | 198.266 | C10H18N2O2 | 95.000 | CC(C)(C)OC(=O)N1C[C@H]2[C@H](N)[C@H]2C1 | 25g | 392627614
EXO-6-AMINO-3-BOC-3-AZABICYCLO[3.1.0]HEXANE | AstaTech | 273206-92-1 | MFCD09832898 | 198.266 | C10H18N2O2 | 95.000 | CC(C)(C)OC(=O)N1C[C@H]2[C@H](N)[C@H]2C1 | 25g | 392627614
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eMolecules 848472-61-7 | 4-(BOC-AMINO)-2-METHYLTHIAZOLE | AstaTech | MFCD27923451 | 214.280 | C9H14N2O2S | 95.000 | Cc1nc(NC(=O)OC(C)(C)C)cs1 | 5g | 458236210
4-(BOC-AMINO)-2-METHYLTHIAZOLE | AstaTech | 848472-61-7 | MFCD27923451 | 214.280 | C9H14N2O2S | 95.000 | Cc1nc(NC(=O)OC(C)(C)C)cs1 | 5g | 458236210
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eMolecules 850568-54-6 | 4-Boc-phenylboronic Acid | Accela ChemBio (ASD) | MFCD03411946 | 222.050 | C11H15BO4 | 95.000 | CC(C)(C)OC(=O)c1ccc(cc1)B(O)O | 5g | 444751008
4-Boc-phenylboronic Acid | Accela ChemBio (ASD) | 850568-54-6 | MFCD03411946 | 222.050 | C11H15BO4 | 95.000 | CC(C)(C)OC(=O)c1ccc(cc1)B(O)O | 5g | 444751008
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eMolecules 39684-80-5 | N-BOC-2-BROMOETHYLAMINE | AstaTech | MFCD02683428 | 224.098 | C7H14BrNO2 | 90.000 | CC(C)(C)OC(=O)NCCBr | 25g | 226993088
N-BOC-2-BROMOETHYLAMINE | AstaTech | 39684-80-5 | MFCD02683428 | 224.098 | C7H14BrNO2 | 90.000 | CC(C)(C)OC(=O)NCCBr | 25g | 226993088
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Medchemexpress LLC N-Hydroxypipecolic acid | 115819-92-6 | 1 ML
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N-Hydroxypipecolic acid is a plant metabolite and a systemic acquired resistance (SAR) regulator. It works in conjunction with the immune signal salicylic acid to establish SAR. This compound accumulates systemically in plant foliage following a pathogen attack and induces SAR against bacterial and oomycete infections. Its mode of action involves directly inducing SAR gene expression, amplifying signals, priming for enhanced defense activation, and positively interacting with salicylic acid signaling to boost plant immunity.
- Molecular weight: 145.16
- Formula: C6H11NO3
- Appearance: Solid
- Color: White to light yellow
- Purity: ≥98.0%
- Structure classification: Ketones, Aldehydes, Acids
- Initial source: Plants other families
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eMolecules 2044702-38-5 | (S)-4-(Boc-amino)-2-(Fmoc-N-methyl-amino)butanoic acid | Advanced ChemBlocks | MFCD30476049 | 454.523 | C25H30N2O6 | 95.000 | CN([C@@H](CCNC(=O)OC(C)(C)C)C(O)=O)C(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 704957673
(S)-4-(Boc-amino)-2-(Fmoc-N-methyl-amino)butanoic acid | Advanced ChemBlocks | 2044702-38-5 | MFCD30476049 | 454.523 | C25H30N2O6 | 95.000 | CN([C@@H](CCNC(=O)OC(C)(C)C)C(O)=O)C(=O)OCC1c2ccccc2-c2ccccc12 | 1g | 704957673
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eMolecules 204058-25-3 | (S)-1-Boc-a-(Fmoc-amino)-4-piperidinepropanoic acid | Acrotein ChemBio Inc. | MFCD01321423 | 494.588 | C28H34N2O6 | 97.000 | CC(C)(C)OC(=O)N1CCC(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)CC1 | 1g | 731674114
(S)-1-Boc-a-(Fmoc-amino)-4-piperidinepropanoic acid | Acrotein ChemBio Inc. | 204058-25-3 | MFCD01321423 | 494.588 | C28H34N2O6 | 97.000 | CC(C)(C)OC(=O)N1CCC(C[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)CC1 | 1g | 731674114
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eMolecules 127828-22-2 | N-Boc-2-(2-aminoethoxy)ethylamine | Accela ChemBio (ASD) | MFCD12031501 | 204.270 | C9H20N2O3 | 97.000 | CC(C)(C)OC(=O)NCCOCCN | 25g | 528276735
N-Boc-2-(2-aminoethoxy)ethylamine | Accela ChemBio (ASD) | 127828-22-2 | MFCD12031501 | 204.270 | C9H20N2O3 | 97.000 | CC(C)(C)OC(=O)NCCOCCN | 25g | 528276735
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eMolecules 1076199-21-7 | N-Boc-2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]ethanamine | Accela ChemBio (ASD) | MFCD09840081 | 356.257 | C13H26BrNO5 | 97.000 | CC(C)(C)OC(=O)NCCOCCOCCOCCBr | 10g | 687211104
N-Boc-2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]ethanamine | Accela ChemBio (ASD) | 1076199-21-7 | MFCD09840081 | 356.257 | C13H26BrNO5 | 97.000 | CC(C)(C)OC(=O)NCCOCCOCCOCCBr | 10g | 687211104
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eMolecules 53292-89-0 | Boc-trans-4-aminocyclohexanecarboxylic acid | A1 Biochem Labs | MFCD01862293 | 243.303 | C12H21NO4 | 95.000 | CC(C)(C)OC(=O)N[C@H]1CC[C@@H](CC1)C(O)=O | 500g | 514314864
Boc-trans-4-aminocyclohexanecarboxylic acid | A1 Biochem Labs | 53292-89-0 | MFCD01862293 | 243.303 | C12H21NO4 | 95.000 | CC(C)(C)OC(=O)N[C@H]1CC[C@@H](CC1)C(O)=O | 500g | 514314864
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Medchemexpress LLC N-(Boc-PEG1)-N-bis(PEG2-propargyl) | 2100306-63-4 | 456.57 | 25 MG
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N-(Boc-PEG1)-N-bis(PEG2-propargyl) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is also a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide 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
- Can be used in the synthesis of PROTACs
- Click chemistry reagent with an alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc)
- Facilitates selective degradation of target proteins
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