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7005-03-0

7005-03-0

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7005-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7005-03-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7005-03:
(6*7)+(5*0)+(4*0)+(3*5)+(2*0)+(1*3)=60
60 % 10 = 0
So 7005-03-0 is a valid CAS Registry Number.

7005-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-2-acetyloxy-1,2-diphenylethenyl] acetate

1.2 Other means of identification

Product number -
Other names (E)-2-(Acetyloxy)-1,2-diphenylethenyl acetate

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:7005-03-0 SDS

7005-03-0Downstream Products

7005-03-0Relevant articles and documents

PALLADIUM-CATALYZED REACTION OF ALLYL CARBAMATES; ALLYLATION OF CARBONUCLEOPHILES, AND PROTECTION-DEPROTECTION OF AMINES

Minami, Ichiro,Ohashi, Yukihiro,Shimizu, Isao,Tsuji, Jiro

, p. 2449 - 2452 (1985)

Allylation of carbonucleophiles with allylic carbamates under neutral conditions has been studied.The C-allylation of carbonucleophile is competitive with the N-allylation of amines, and the structure of amines is crucial for the selectivity.Bulky secondary amines gave the best results.Also a new method of protection-deprotection of amines as carbamates has been developed.Smooth deprotection is possible by the palladium-catalyzed reaction of allyl carbamates with formic acid.This method is particulary useful for primary amines, including optically active amino acids.

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