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25355-30-0

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25355-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25355-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,5 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25355-30:
(7*2)+(6*5)+(5*3)+(4*5)+(3*5)+(2*3)+(1*0)=100
100 % 10 = 0
So 25355-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-2-6(5-8)3-4-7/h4-6H,2-3H2,1H3

25355-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylbutanedial

1.2 Other means of identification

Product number -
Other names Ethylsuccinaldehyde

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:25355-30-0 SDS

25355-30-0Downstream Products

25355-30-0Relevant articles and documents

Evidence for isomerizing hydroformylation of butadiene. A combined experimental and computational study

Maji, Tapan,Mendis, Camina H.,Thompson, Ward H.,Tunge, Jon A.

, p. 145 - 152 (2016/09/09)

The (DIOP)rhodium-catalyzed hydroformylation of butadiene has been shown to give among the highest selectivities for formation of adipaldehyde, which is useful for the synthesis of nylon. Herein, isomerizing hydroformylation is shown to be a mechanism that is partially responsible for this selectivity and density functional theory studies are used to reveal the detailed pathway for the requisite alkene isomerization.

Process for the preparation of 2-alkyl-1,4-butanedial

-

, (2008/06/13)

A process is disclosed for the preparation of 2-alkyl-1,4-butanedial by hydroformylation of acetals of a 2-alkyl-substituted-1-propenal in the presence of a complex rhodium catalyst. The 3-alkyl-4,4-dialkoxybutanal obtained in this manner is separated and hydrolyzed to the desired compound.

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