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81168-89-0

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81168-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81168-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,6 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81168-89:
(7*8)+(6*1)+(5*1)+(4*6)+(3*8)+(2*8)+(1*9)=140
140 % 10 = 0
So 81168-89-0 is a valid CAS Registry Number.

81168-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 16-bromohexadec-5-en-9-yne

1.2 Other means of identification

Product number -
Other names 5-Hexadecen-9-yne,16-bromo-,(Z)

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:81168-89-0 SDS

81168-89-0Downstream Products

81168-89-0Relevant articles and documents

Alkynyl halide compounds and alkenyl acetate compounds therefrom

-

, (2008/06/13)

The invention provides a novel method for the synthetic preparation of an ω-haloalkyne compound of the general formula R--C C--CH2)n X, in which X is a halogen atom, R is a monovalent hydrocarbon group and n is 4, 5 or 6, by the coupling reaction of a Grignard reagent RMgX' and an ω-halo-1-bromoalkyne compound of the formula X--CH2)n C C-Br. The ω-haloalkyne compound obtained in the above can be readily converted to the corresponding alkenyl acetate of the formula R--CH=CH--CH2)n OCOCH3 by first acetylating and then partially hydrogenating in the presence of a Lindlar catalyst. In particular, 7, 11-hexadecadienyl acetate, which is a sexual pheromone compound of a noxious insect, is obtained in the same route of synthesis starting with the Grignard reagent of a 1-halo-3-octene and 1, 8-dibromo-1-octyne.

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