93371-30-3

Basic information

• Product Name: (S)-3-(Boc-aMino)-1-chloro-2-butanone
• Synonyms: (S)-3-(Boc-aMino)-1-chloro-2-butanone;(S)-tert-butyl (4-chloro-3-oxobutan-2-yl)carbamate;tert-butyl(S)-(4-chloro-3-oxobutan-2-yl)carbamate;EOS-60778
• CAS NO: 93371-30-3
• Molecular Formula: C9H16ClNO3
• Molecular Weight: 221.68124
• Mol File: 93371-30-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (S)-3-(Boc-aMino)-1-chloro-2-butanone(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-(Boc-aMino)-1-chloro-2-butanone(93371-30-3)
• EPA Substance Registry System: (S)-3-(Boc-aMino)-1-chloro-2-butanone(93371-30-3)

Safety Data

• Hazardous Substances Data: 93371-30-3(Hazardous Substances Data)

Usage

General Description

(S)-3-(Boc-amino)-1-chloro-2-butanone is a chemical compound that is commonly used in organic synthesis. It is a chiral compound with a Boc-protected amino group and a chlorine atom attached to a butanone moiety. (S)-3-(Boc-aMino)-1-chloro-2-butanone is often used as a building block in the synthesis of pharmaceuticals and other biologically active compounds.

Upstream product

• 593-71-5 Chloroiodomethane 
• 28875-17-4 (S)-N-(tert-butoxycarbonyl)alanine methyl ester 
• 51814-53-0 N-tert-butoxycarbonyl-L-alanine ethyl ester 
• 67919-80-6 (S)-3-[(tert-butoxy)carbonylamino]-1-diazobutan-2-one 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 126027-07-4 tert-butyl N-[(1S)-1-methyl-2-oxo-propyl]carbamate 
• 165683-88-5 (S)-1-<(S)-1-(tert-butoxycarbonylamino)ethyl>oxirane 

Relevant articles and documents

SUBSTITUTED 3-AZABICYCLO[3.1.0]HEXANES AS KETOHEXOKINASE INHIBITORS

Provided herein are substituted 3-azabicyclo[3.1.0]hexanes as ketohexokinase inhibitors, processes to make said compounds, and methods comprising administering said compounds to a mammal in need thereof.

A practical method for the preparation of α'-chloroketones of N-carbanaate protected-α-aminoacids

A practical method for the preparation of α-N-BOC-epoxides from protected amino acid esters based on the Kowalski homologation reaction is described. This procedure can be readily performed on a large scale without the use of hazardous reagents and has allowed preparation of epoxides 3 in multi-kilogram quantities.