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120671-12-7

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120671-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120671-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,6,7 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120671-12:
(8*1)+(7*2)+(6*0)+(5*6)+(4*7)+(3*1)+(2*1)+(1*2)=87
87 % 10 = 7
So 120671-12-7 is a valid CAS Registry Number.

120671-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2-(ethoxycarbonylmethylene)-2,3,4,5-tetrahydroimidazole

1.2 Other means of identification

Product number -
Other names (E)-2-(ethoxycarbonylmethylene)-1-benzylimidazoline

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:120671-12-7 SDS

120671-12-7Relevant articles and documents

The aza-ene or the Michael addition? Examination of an unusual substituent effect on the reaction of heterocyclic ketene aminals with ethyl propiolate

Zhao, Mei-Xin,Wang, Mei-Xiang,Huang, Zhi-Tang

, p. 1309 - 1316 (2007/10/03)

Heterocyclic ketene aminals having at least one secondary amino group underwent the aza-ene reaction with ethyl propiolate under various conditions to yield the corresponding adducts, which were readily transformed into the δ-lactam fused heterocyclic products with or without the aid of sodium ethoxide in refluxing ethanol, while the ester- and cyano-substituted tertiary enediamines acted as the strong Michael donor to add to ethyl propiolate in a polar or a protic solvent. The unusual substituent effect on the reactivity and mechanism was discussed.

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