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Ethenamine, N,N-dimethyl-2-(2,6,6-trimethyl-1-cyclohexen-1-yl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106175-65-9

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106175-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106175-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,7 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106175-65:
(8*1)+(7*0)+(6*6)+(5*1)+(4*7)+(3*5)+(2*6)+(1*5)=109
109 % 10 = 9
So 106175-65-9 is a valid CAS Registry Number.

106175-65-9SDS

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 (1E)-2-(2',6',6'-trimethylcyclohex-1'-enyl)-N,N-dimethylethen-1-ylamine

1.2 Other means of identification

Product number -
Other names Dimethyl-[(E)-2-(2,6,6-trimethyl-cyclohex-1-enyl)-vinyl]-amine

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:106175-65-9 SDS

106175-65-9Relevant academic research and scientific papers

98. A Regioselective Cyclohexannulation Procedure via Dienamine Cycloaddition. Synthesis of Functionalised Decalins

Snowden, Roger L.,Linder, Simon M.,Wuest, Manfred

, p. 892 - 905 (2007/10/02)

A regioselective cyclohexannulation procedure, whose key step involves the cycloaddition of dienamines 12-24 with methyl acrylate, allows the conversion of cycloalkanones 1-11 to bicyclic dienoates 25-37.The chemistry of 26 is briefly examined and, in the context of organoleptic studies concerning functionalised 5,5,9-trimethyldecalins, the transformation of 37 to ketones 44 and 46 as well as to acetates 53-56 is described.

DIENAMINES AS DIELS-ALDER DIENES. AN EFFICIENT CYCLOHEXANNULATION SEQUENCE.

Snowden, Roger L.,Wuest, Manfred

, p. 699 - 702 (2007/10/02)

An efficient cyclohexannulation sequence is described whose key step involves a Diels-Alder reaction between an (E)-dienamine and methyl acrylate.

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