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1,5-Cyclohexadiene-1-carboxaldehyde, 5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88967-15-1

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88967-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88967-15-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88967-15:
(7*8)+(6*8)+(5*9)+(4*6)+(3*7)+(2*1)+(1*5)=201
201 % 10 = 1
So 88967-15-1 is a valid CAS Registry Number.

88967-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylcyclohexa-1,5-diene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names dihydrotoluylaldehyde

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:88967-15-1 SDS

88967-15-1Upstream product

88967-15-1Downstream Products

88967-15-1Relevant academic research and scientific papers

SIDE REACTION IN THE ALDOL CONDENSATION OF ACETALDEHYDE

Nikitina, L. I.,Katsnel'son, M. G.,Kagna, S. Sh.,Skop, S. L.,Rabinovich, A. S.,Sysoeva, G. A.

, p. 2003 - 2006 (2007/10/02)

It was established that the main side products in the condensation of acetaldehyde in the presence of cobalt naphthenate are 3-hydroxybutanal, 2,4- and 2,5-hexadienal, the monoacetate of 1,3-butanediol, and dihydrotoluylaldehyde.From the proposed scheme of side reactions it follows that the majority of the side products are formed in the reaction of 3-hydroxybutanal with acetaldehyde.Realization of the process at an increased temperature with a low initial concentration of acetaldehyde and for short contact times makes it possible to reduce the yield of the side products.

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