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87519-21-9

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87519-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87519-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,1 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87519-21:
(7*8)+(6*7)+(5*5)+(4*1)+(3*9)+(2*2)+(1*1)=159
159 % 10 = 9
So 87519-21-9 is a valid CAS Registry Number.

87519-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-dimethyl-2(E),6-octadienyl (phenylthio)acetate

1.2 Other means of identification

Product number -
Other names Phenylsulfanyl-acetic acid (E)-3,7-dimethyl-octa-2,6-dienyl ester

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:87519-21-9 SDS

87519-21-9Relevant articles and documents

Sythesis of Two Macrolide Pheromones of the Rusty Grain Beetle, Cryptolestes ferrugineus (Stephens)

Oehlschlager, Allan C.,Wong, John W.,Verigin, Victor G.,Pierce, Harold D.

, p. 5009 - 5017 (1983)

Two macrolide pheromones for Cryptolestes ferrugineus (Stephens), the rusty grain beetle, have been synthesized.Synthesis of 4,8-dimethyl-4(E),8(E)-decadienolide (1) was achived by intramolecular alkylation of an ω-bromo (phenylthio)acetate derived from geraniol by reaction with (phenylthio)acetyl choride and allylic functionalization of the 8(E)-methyl.Macrolide 1 was also synthesized by intramolecular esterification of an ω-hydroxy acid derived from geraniol by formal addition of acetate to tetrahydroparanyl-protected 8(E)-bromogeraniol.Synthesis of the second macrolide, 11-methyl-3(Z)-undecenolide (2), also involved intramolecular esterification of the appropriate hydroxy acid.The chiral center of 2 was introduced via chiral propylene oxides while the Z unsaturation was introduced by P-2 nickel reduction of the appropriate alkyne.Both chiral isomers of 2 were synthesized.

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