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1,1'-Biphenyl, 4-(1-propynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61948-01-4

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61948-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61948-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,4 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61948-01:
(7*6)+(6*1)+(5*9)+(4*4)+(3*8)+(2*0)+(1*1)=134
134 % 10 = 4
So 61948-01-4 is a valid CAS Registry Number.

61948-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4-prop-1-ynylbenzene

1.2 Other means of identification

Product number -
Other names 1,1'-Biphenyl,4-(1-propynyl)

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:61948-01-4 SDS

61948-01-4Relevant academic research and scientific papers

Organomagnesium-catalyzed isomerization of terminal alkynes to allenes and internal alkynes

Rochat, Rapha?l,Yamamoto, Koji,Lopez, Michael J.,Nagae, Haruki,Tsurugi, Hayato,Mashima, Kazushi

, p. 8112 - 8120 (2015)

Organomagnesium complexes 2 were synthesized from N,N-dialkylamineimine ligands 1 and dibenzylmagnesium by benzylation of the imine moiety. 3-Aryl-1-propynes reacted with 2 to form the corresponding tetraalkynyl complexes, which acted as catalysts for the transformation of these terminal alkynes into allenes and further to internal alkynes under mild conditions. To the best of our knowledge, this example is the first of an organomagnesium-catalyzed isomerization of alkynes. Notably, the reactions proceeded through temporally separated autotandem catalysis, thus allowing the isolation of the allene or internal alkyne species in good yields. Mechanistic experiments suggested that the catalytically active tetraalkynyl complexes consist of a tautomeric mixture of alkynyl-, allenyl-, and propargylmagnesium species.

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