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29079-00-3

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29079-00-3 Usage

Uses

Different sources of media describe the Uses of 29079-00-3 differently. You can refer to the following data:
1. 4-?Ethynyl-?1,?1'-?biphenyl is a general reagent used in the alkynylation of indoles and C1 alkynylation of carbazoles. Also used in the synthesis of [3,2=c]coumarin derivatives using visible-light-promoted radical alkyne insertion.
2. 4-?Ethynyl-?1,?1''-?biphenyl is a general reagent used in the alkynylation of indoles and C1 alkynylation of carbazoles. Also used in the synthesis of [3,2=c]coumarin derivatives using visible-light-promoted radical alkyne insertion.

Check Digit Verification of cas no

The CAS Registry Mumber 29079-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 29079-00:
(7*2)+(6*9)+(5*0)+(4*7)+(3*9)+(2*0)+(1*0)=123
123 % 10 = 3
So 29079-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H10/c1-2-12-8-10-14(11-9-12)13-6-4-3-5-7-13/h1,3-11H

29079-00-3 Well-known Company Product Price

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  • Aldrich

  • (521175)  4-Ethynylbiphenyl  97%

  • 29079-00-3

  • 521175-5G

  • 1,869.66CNY

  • Detail

29079-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ETHYNYL-1,1'-BIPHENYL

1.2 Other means of identification

Product number -
Other names 4-ETHYNYLBIPHENYL

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:29079-00-3 SDS

29079-00-3Upstream product

29079-00-3Relevant articles and documents

A mechanistic study of the chromium(II)-mediated transformations of trichloromethyl alkyls and carbinols: evidence for carbene, carbyne, and carbenoid intermediates

Bejot, Romain,Tisserand, Steve,Li, De Run,Falck,Mioskowski, Charles

, p. 3855 - 3858 (2008/02/02)

Using CrCl2 in THF at room temperature, trichloromethyl carbinols and trichloromethylalkanes are readily transformed to the highly reactive α-chlorocarbenes, carbynes and α-chloro-α-chromium(III) vinylidene carbenoids. A mechanistic study is carried out to determine the nature of the intermediates.

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