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66582-16-9

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66582-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66582-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66582-16:
(7*6)+(6*6)+(5*5)+(4*8)+(3*2)+(2*1)+(1*6)=149
149 % 10 = 9
So 66582-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO/c1-5(2)3-6(8)4-7/h5H,3H2,1-2H3

66582-16-9SDS

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 3-methylbutanoyl cyanide

1.2 Other means of identification

Product number -
Other names 4-Methyl-2-oxopentanenitrile

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:66582-16-9 SDS

66582-16-9Relevant articles and documents

PROCESS FOR THE PREPARATION OF ( S ) - 3 - CYANO - 5 - METHYLHEXANOIC ACID DERIVATIVES ADN OF PREGABALIN

-

Page/Page column 24-25, (2012/03/26)

The invention provides a process for the manufacture of a compound of formula (I) using an enzyme catalysed reduction of a compound of formula (lla) or llb). Compounds of formula (I) are useful for preparing pregabalin.

Trimethylsilyl Cyanide - A Reagent for Umpolung, VIII. Derivatives of 2-(Trimethylsilyloxy)-2-propenenitrile. Syntheses and General Properties

Hertenstein, Ulrich,Huenig, Siegfried,Reichelt, Helmut,Schaller, Rainer

, p. 261 - 287 (2007/10/02)

Rather different derivatives of the new title compuond 7 were synthesized by routes A - H (Table 2 and 3).The effects of substituents and reaction routes on the E/Z ratios (NMR) is discussed.Replacement of SiMe3 in 7 by RCO- and MeSO2- yields other alkenes with donor (O - X) and acceptor groups (CN) at the same C-atom.Their opposite effects on the β-C-atom is estimated from the corresponding 1H- and 13C-NMR signals.

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