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Benzenamine, 4-(1,3,6-cycloheptatrien-1-yl)-N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30366-75-7

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30366-75-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30366-75-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30366-75:
(7*3)+(6*0)+(5*3)+(4*6)+(3*6)+(2*7)+(1*5)=97
97 % 10 = 7
So 30366-75-7 is a valid CAS Registry Number.

30366-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyclohepta-1,3,6-trien-1-yl-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names p-Dimethylaminophenyl-cycloheptatrien

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:30366-75-7 SDS

30366-75-7Relevant academic research and scientific papers

Base-catalysed isomerization of 7-phenyl-1,3,5-cycloheptatriene

Zwaard, A. W.,Prins, M. D.,Kloosterziel, H.

, p. 188 - 192 (2007/10/02)

Under the influence of basic alcohol, 7-phenyl-1,3,5-cycloheptatriene (7c) forms its 1-, 2- and 3-isomers (viz. 1c, 2c and 3c) in parallel reactions, contrary to suggestions made in the literature.The activation parameters for these reactions are given.The difference in behaviour (in isomerization and exchange reactions under basic conditions) between 7-(methoxycarbonyl)-1,3,5-cycloheptatriene (7b) and 7-phenyl-1,3,5-cyclopentatriene (7c) is explained by the weaker electron-attracting properties of the phenyl ring as compared to the methoxycarbonyl substituent.

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