10342-06-0

Basic information

• Product Name: N-[tert-butoxycarbonyl]-L-serine, compound with dicyclohexylamine (1:1)
• Synonyms: N-(tert-Butoxycarbonyl)-L-serine, compound with dicyclohexylamine (1:1); (2S)-2-(tert-butoxycarbonylamino)-3-hydroxy-propanoic acid; N-cyclohexylcyclohexanamine
• CAS NO: 10342-06-0
• Molecular Formula: C₈H₁₅NO₅*C₁₂H₂₃N
• Molecular Weight: 386.5261
• EINECS: 233-742-0
• Mol File: 10342-06-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 562°C at 760 mmHg
• Flash Point: 293.7°C
• Vapor Pressure: 5.72E-15mmHg at 25°C
• CAS DataBase Reference: N-[tert-butoxycarbonyl]-L-serine, compound with dicyclohexylamine (1:1)(CAS DataBase Reference)
• NIST Chemistry Reference: N-[tert-butoxycarbonyl]-L-serine, compound with dicyclohexylamine (1:1)(10342-06-0)
• EPA Substance Registry System: N-[tert-butoxycarbonyl]-L-serine, compound with dicyclohexylamine (1:1)(10342-06-0)

Safety Data

• Hazardous Substances Data: 10342-06-0(Hazardous Substances Data)

Usage

General Description

N-[tert-butoxycarbonyl]-L-serine, compound with dicyclohexylamine (1:1) is a chemical compound that consists of one molecule of N-[tert-butoxycarbonyl]-L-serine and one molecule of dicyclohexylamine in a 1:1 ratio. It is commonly used as a protecting group for the amino acid serine and is often employed in peptide synthesis to prevent unwanted reactions at the amino group. The compound is also utilized in the manufacturing of pharmaceuticals, specifically in the production of peptide-based drugs. Additionally, it may have applications in the field of organic chemistry and biochemistry for its ability to modify and study the properties of serine-containing molecules.

Upstream product

• 59524-02-6 N-tert-butoxycarbonyl-L-serine benzyl ester 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 147-85-3 L-proline 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 120219-31-0 L-N-(tert-butoxycarbonyl)serine phenacyl ester 

Relevant articles and documents

Peptide synthesis in aqueous solution. IV. Preparation and properties of [p-(benzyloxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate, [p-(t-butoxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate and [p-(9-fluorenylmethyl-oxycarbonyloxy)phenyl]dimethylsulfonium methyl sulfate as water-soluble N-acylating reagents

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