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1,3-Cycloheptadiene, 1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14947-22-9

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14947-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14947-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,4 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14947-22:
(7*1)+(6*4)+(5*9)+(4*4)+(3*7)+(2*2)+(1*2)=119
119 % 10 = 9
So 14947-22-9 is a valid CAS Registry Number.

14947-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylcyclohepta-1,3-diene

1.2 Other means of identification

Product number -
Other names 1-methyl-1,3-cycloheptadiene

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:14947-22-9 SDS

14947-22-9Downstream Products

14947-22-9Relevant academic research and scientific papers

Rearrangements of 1-Cyclohexenylmethylenes and Their Relevance to the Mechanism of the Phenylcarbene Rearrangement

Miller, Paula C.,Gaspar, Peter P.

, p. 5101 - 5107 (2007/10/02)

Gas-phase pyrolysis of 1-cyclohexenyldiazomethane (17) and (2-methyl-1-cyclohexenyl)diazomethane (36) leads to the generation of cyclohexenylmethylenes, 13 and 27, respectively, whose intramolecular rearrangement mechanism can be inferred from the stable end products.These substituted vinylmethylenes undergo intramolecular ?-addition, but apparently do not participate in all-carbon Wolff rearrangement.The relevance of these results to the mechanism of the phenylcarbene rearrangement is discussed, and it is suggested that a ?-route with a bicycloheptatriene-like transition state may operate.An attempt to generate 1,3-cyclohexadienylmethylene is described.

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