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757959-97-0

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757959-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 757959-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,9,5 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 757959-97:
(8*7)+(7*5)+(6*7)+(5*9)+(4*5)+(3*9)+(2*9)+(1*7)=250
250 % 10 = 0
So 757959-97-0 is a valid CAS Registry Number.

757959-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-acetamido-4-methylhexanoic acid

1.2 Other means of identification

Product number -
Other names N-ACETYL-4-METHYL-NORLEUCINE

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:757959-97-0 SDS

757959-97-0Downstream Products

757959-97-0Relevant articles and documents

ON THE CATALYTIC AMIDOCARBONYLATION OF SUBSTITUTED ALLYLIC ALCOHOLS

Yuan, Sun-Shine,Ajami, Alfred M.

, p. 255 - 258 (2007/10/02)

Substituted allylic alcohols (3-methyl-2-buten-1-ol and 2-methyl-3-buten-2-ol) were isomerized and amidocarbonylated.In addition to the expected product, N-acetylleucine, arising from their rearrengement to 3-methylbutanal and subsequent amidocarbonylation (22percent yield), we isolated two additional products (28percent yield).These were shown by spectroscopic methods and by syntheses, via amidocarbonylations of the respective aldehydes, to be 2-acetamido-5-methylhexanoic acid and 2-acetamido-4-methylhexanoic acid.Their formation is postulated to be the sequential result of (i) dehydration first to form isoprene, (ii) hydroformylation and hydrogenation of isoprene to give 3-methyl-1-pentanal and 4-methyl-1-pentanal, and (iii) aldehyde amidocarbonylation.Treatment of isoprene itself under the same conditions also gave these latter two acetylamino acids.

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