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2-Propenoic acid, 3-(4-methoxy-2-methylphenyl)-, ethyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100606-37-9

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100606-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100606-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,0 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 100606-37:
(8*1)+(7*0)+(6*0)+(5*6)+(4*0)+(3*6)+(2*3)+(1*7)=69
69 % 10 = 9
So 100606-37-9 is a valid CAS Registry Number.

100606-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-(4-methoxy-2-methylphenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names ethyl (E)-3-(4-methoxy-2-methylphenyl)-2-propenoate

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:100606-37-9 SDS

100606-37-9Downstream Products

100606-37-9Relevant academic research and scientific papers

Cycloalkyl alkanoic acids as integrin receptor antagonists derivatives

-

Page 36-37, (2010/02/07)

The present invention relates to a class of compounds represented by the Formula I or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of the Formula I, and methods of selectively inhibiting or antagonizing the αvβ3 and/or αvβ5 integrin.

Synthesis of Substituted 1,2-Dihydroisoquinolines by the Intramolecular 1,3-Dipolar Alkyl Azide-Olefin Cycloaddition

Liu, Jia-Ming,Young, Jenn-Jong,Li, Yu-Jang,Sha, Chin-Kang

, p. 1120 - 1123 (2007/10/02)

A general synthesis of substituted 1,2-dihydroisoquinolines based on intramolecular 1,3-dipolar cycloaddition of alkyl azides and olefins is described.Reaction of bromide 4 with sodium azide afforded azide 5, which underwent 1,3-dipolar cycloaddition intramolecularly to give triazoline 6 .Rearrangement of triazoline 6 on silica gel gave diazo compound 7.Treatment of 7 with rhodium acetate afforded substituted 1,2-dihydroisoquinoline 9 in good overall yield.

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