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2,3-Butanediol, 2-methyl-, (S)-, also known as (S)-2-methyl-2,3-butanediol, is a chiral chemical compound with the molecular formula C5H12O2. It is a colorless liquid and possesses a stereocenter, making it a unique molecule in the realm of chemistry. 2,3-Butanediol, 2-methyl-, (S)is relatively safe and finds wide-ranging applications in various industries due to its versatile properties.

24347-59-9

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24347-59-9 Usage

Uses

Used in Solvent Applications:
2,3-Butanediol, 2-methyl-, (S)is used as a solvent for various chemical reactions and processes due to its ability to dissolve a wide range of substances and facilitate reactions.
Used in Flavoring and Fragrance Industry:
2,3-Butanediol, 2-methyl-, (S)is used as a flavoring agent and in the production of fragrances, adding unique scents and enhancing the sensory experience of various products.
Used in Pharmaceutical Synthesis:
2,3-Butanediol, 2-methyl-, (S)is used in the synthesis of pharmaceuticals, serving as a key intermediate in the production of various drugs and medicinal compounds.
Used as a Precursor in Chemical Production:
2,3-Butanediol, 2-methyl-, (S)is used as a precursor in the production of other chemicals, contributing to the synthesis of a diverse array of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 24347-59-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24347-59:
(7*2)+(6*4)+(5*3)+(4*4)+(3*7)+(2*5)+(1*9)=109
109 % 10 = 9
So 24347-59-9 is a valid CAS Registry Number.

24347-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-methyl-2,3-butanediol

1.2 Other means of identification

Product number -
Other names -

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:24347-59-9 SDS

24347-59-9Downstream Products

24347-59-9Relevant academic research and scientific papers

Desamination of β- and γ-Amino Alcohols

Guenther, Bernd-Rainer,Kirmse, Wolfgang

, p. 518 - 532 (2007/10/02)

Nitrous acid deaminations of the β-amino alcohols 2 and 12 afford 1,2 diols as well as ketones by pinacolic rearrangement.Both types of products arise with predominant inversion of configuration.Stereochemical studies and isotopic labeling reveal that formation of the diols involves an oxygen shift, presumably via oxirane intermediates.Deamination of the γ-amino alcohol 37 induces, in part, sequential rearrangements to give products also obtained from 12, but in different proportions and enantiomeric purities.Conformational control provides a reasonable explanation of our results.

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