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97856-56-9

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97856-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97856-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97856-56:
(7*9)+(6*7)+(5*8)+(4*5)+(3*6)+(2*5)+(1*6)=199
199 % 10 = 9
So 97856-56-9 is a valid CAS Registry Number.

97856-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-cyclohexylidenebut-2-enoate

1.2 Other means of identification

Product number -
Other names 4-cyclohexylidene-trans-crotonic acid ethyl ester

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:97856-56-9 SDS

97856-56-9Relevant articles and documents

Facile preparation of cyclopropanes from 2-iodoethyl-substituted olefins and 1,3-dihalopropanes with zinc powder

Sakuma, Daisuke,Togo, Hideo

, p. 10138 - 10145 (2007/10/03)

Two efficient, simple, cheap, and environmentally benign preparations of cyclopropanes were achieved. One is the formation via 3-exo-trig manner from various electron-deficient 2-iodoethyl-substituted olefins with zinc powder in a mixture of t-butyl alcoh

Practical Stereoselective Synthesis of (2E)- and (2Z)-4-Cycloalkylidenebut-2-enoic Acids

Karagiozov, Stoyan K.,Abbott, Frank S.

, p. 871 - 888 (2007/10/03)

Stereoselective synthesis of α,β-unsaturated esters 7 and 8 was achieved through Horner-Wadsworth-Emmons reaction of β,β -disubstituted α,β-unsaturated aldehydes. Thus, aldehydes 6 undergo olefination with phosphonate carbanion generated from triethyl phosphonoacetate 3 and lithium hydroxide or butyl lithium/DMPU to give (E)-α,β -unsaturated esters 7 with excellent selectivity. The treatment of 6 with the new Horner-Emmons reagents, ethyl(diphenylphosphono)acetate 4a and ethyl (di-o-tolyl-phosphono) acetate 4b in the presence of benzyltrimethyl ammonium hydroxide (Triton B) afforded (Z)-α,β-unsaturated esters 8 with 73-89% selectivity. The esters 7 and 8 were converted to (2E)- and (2Z)-4-cycloalkylidenebut-2-enoic acids 9 and 10, respectively.

A Facile Synthesis of 2,4-Alkadienoic Esters and 2,4,6-Alkatrienoic Esters via Arsonium Ylides

Huang, Yaozeng,Shen, Yanchang,Zheng, Jianhua,Zhang, Shixiang

, p. 57 - 58 (2007/10/02)

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