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40650-87-1

40650-87-1

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40650-87-1 Usage

Chemical Properties

Yellow Crystalline Solid

Uses

Deca-2,4,6,8-tetraenal (cas# 40650-87-1) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 40650-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,5 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40650-87:
(7*4)+(6*0)+(5*6)+(4*5)+(3*0)+(2*8)+(1*7)=101
101 % 10 = 1
So 40650-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O/c1-2-3-4-5-6-7-8-9-10-11/h2-10H,1H3/b3-2+,5-4+,7-6+,9-8+

40650-87-1SDS

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 Deca-2,4,6,8-tetraenal

1.2 Other means of identification

Product number -
Other names DECA-2,4,6,8-TETRAENAL

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:40650-87-1 SDS

40650-87-1Downstream Products

40650-87-1Relevant articles and documents

Catalytic Reactions of Homo- and Cross-Condensation of Ethanal and Propanal

Martsinkevich,Bruk,Dashko,Afaunov,Flid,Sedov

, p. 1032 - 1035 (2019/01/03)

Abstract: Processes of catalytic homocondensation of propanal and its cross-condensation with ethanal and methanal in the presence of aniline and amino acids have been studied. The dependence of the conversion of the reactants and selectivity of the homo/heterocondensation process on the catalyst nature and temperature has been revealed. It has been shown that the maximum acrolein selectivity is reached in the case of using benzoyl-substituted derivatives in water, with the proportion of the products of further condensation decreasing. The selectivity for the ethanal homocondensation product 2-butenal decreases simultaneously as a result of the formation of linear and branched oligomers of successive condensation.

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