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70964-99-7

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70964-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70964-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,9,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70964-99:
(7*7)+(6*0)+(5*9)+(4*6)+(3*4)+(2*9)+(1*9)=157
157 % 10 = 7
So 70964-99-7 is a valid CAS Registry Number.

70964-99-7SDS

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 acetic acid,2-prop-2-enoxyethanol

1.2 Other means of identification

Product number -
Other names Essigsaeure-(2-allyloxy-aethylester)

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:70964-99-7 SDS

70964-99-7Downstream Products

70964-99-7Relevant articles and documents

Diphilic carbosilane dendrimers with different densities of the hydrophilic layer

Getmanova,Tereshchenko,Ignat'eva,Tatarinova,Myakushev,Muzafarov

, p. 137 - 143 (2004)

A universal method for the synthesis of hydrophilic dendrimers was considered. The method is based on a combination of carbosilane dendrimers with different molecular organizations and hydrophilizing agents, viz., substituted hydride silanes containing one and three protected hydroxyl groups. The combination of a limited set of the mentioned reagents makes it possible to control the ratio of hydrophilic and hydrophobic moieties of the molecular structure in wide limits. A simple and convenient method for the removal of trimethylsilyl protection of hydroxyl groups in the surface layer of dendrimers was developed.

Ruthenium(III) chloride catalyzed acylation of alcohols, phenols, thiols, and amines

Kanta De, Surya

, p. 2919 - 2922 (2007/10/03)

Ruthenium(III) chloride catalyzes the acylation of a variety of phenols, alcohols, thiols, and amines under mild conditions. Some of the major advantages of this method are high yields, short reaction times, ease of operation, and compatibility with other protecting groups.

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