26988-59-0

Basic information

• Product Name: Boc-Cys(Trt)-OH DCHA
• Synonyms: Boc-Cys(Trt)-OH DCHA;DicyclohexylaMine (R)-2-((tert-butoxycarbonyl)aMino)-3-(tritylthio)propanoate;N-[(1,1-Dimethylethoxy)carbonyl]-S-(triphenylmethyl)-L-cysteine compd. with N-cyclohexylcyclohexanamine;(Tert-Butoxy)Carbonyl Cys(Trt)-OH·DCHA
• CAS NO: 26988-59-0
• Molecular Formula: C₁₂H₂₃N*C₂₇H₂₉NO₄S
• Molecular Weight: 644.90618
• EINECS: -0
• Mol File: 26988-59-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Boc-Cys(Trt)-OH DCHA(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-Cys(Trt)-OH DCHA(26988-59-0)
• EPA Substance Registry System: Boc-Cys(Trt)-OH DCHA(26988-59-0)

Safety Data

• Hazardous Substances Data: 26988-59-0(Hazardous Substances Data)

Usage

General Description

Boc-Cys(Trt)-OH DCHA is a chemical compound composed of three key components: Boc, Cys(Trt), and DCHA. Boc, or t-butoxycarbonyl, is a protective group used to block the reactivity of certain functional groups in organic chemistry. Cys(Trt) refers to the amino acid cysteine with a trityl-protected thiol group. The trityl group is a bulky protecting group used in peptide synthesis to shield the thiol group from unwanted reactions. DCHA, or diisopropylcarbodiimide-hydroxybenzotriazol, is a coupling reagent used to facilitate peptide bond formation in organic synthesis. Together, these components work in concert to help chemists to efficiently synthesize complex peptides and proteins in the laboratory.

Upstream product

• 34619-03-9 tert-butyldicarbonate 
• 2799-07-7 S-trityl-L-cysteine 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 77-92-9 citric acid 
• 58632-95-4 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile 

Downstream Products

• 118002-46-3 phenceptin 
• 118039-05-7 N-Boc-S-trityl-L-cysteinyl-glycyl-L-prolyl-glycyl-L-prolyl-S-trityl-L-cysteine benzhydryl ester 

Relevant articles and documents

Phenceptin: A biomimetic model of the phenytoin receptor

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