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173472-42-9

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173472-42-9 Usage

General Description

(S)-3-BOC-AMINO-1-DIAZO-5-METHYLTHIO-2-PENTANONE is a chemical compound that belongs to the class of diazo compounds. It is a white crystalline powder that is used in organic synthesis as a reagent for the preparation of various organic compounds. The Boc-amino group in the molecule provides protection for the amino functionality during chemical reactions, while the diazo and methylthio groups contribute to its reactivity and selectivity in different types of reactions. (S)-3-BOC-AMINO-1-DIAZO-5-METHYLTHIO-2-PENTANONE is commonly used in the pharmaceutical industry for the synthesis of drug intermediates and active pharmaceutical ingredients. However, it is important to handle and use this compound with caution due to its potential hazards and risks associated with diazo compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 173472-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 173472-42:
(8*1)+(7*7)+(6*3)+(5*4)+(4*7)+(3*2)+(2*4)+(1*2)=139
139 % 10 = 9
So 173472-42-9 is a valid CAS Registry Number.

173472-42-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-BOC-AMINO-1-DIAZO-5-METHYLTHIO-2-PENTANONE

1.2 Other means of identification

Product number -
Other names tert-butyl N-{(1S)-3-diazo-1-[2-(methylsulfanyl)ethyl]-2-oxopropyl}carbamate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:173472-42-9 SDS

173472-42-9Relevant articles and documents

Synthesis of enantiopure dehydropiperidinones from α-amino acids and alkynes via azetidin-3-ones

Ishida, Naoki,Yuhki, Tatsuya,Murakami, Masahiro

supporting information; experimental part, p. 3898 - 3901 (2012/09/22)

Chiral dehydropiperidinones were synthesized in enantiopure form from α-amino acids and alkynes via azetidin-3-ones.

The synthesis of di(hydroxyalkyl) substituted bicyclic guanidines

Madder, A.,Muenster, I.,Rolle, U.,Clercq, P. J. De

, p. 613 - 622 (2007/10/03)

The synthesis of the enantiomerically pure bicyclic guanidines 3a and 3b is described.The convergent strategy is based on methodology developed by Schmidtchen.The therefore required amine components 6 and 9 obtained from methionine and L-glutamic acid, respectively.

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