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6712-35-2

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6712-35-2 Usage

Synthesis Reference(s)

Tetrahedron Letters, 34, p. 15, 1993 DOI: 10.1016/S0040-4039(00)60046-1

Check Digit Verification of cas no

The CAS Registry Mumber 6712-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6712-35:
(6*6)+(5*7)+(4*1)+(3*2)+(2*3)+(1*5)=92
92 % 10 = 2
So 6712-35-2 is a valid CAS Registry Number.

6712-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (+/-)-2-phenylpent-4-yn-2-ol

1.2 Other means of identification

Product number -
Other names 2-Phenyl-pent-4-in-2-ol

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:6712-35-2 SDS

6712-35-2Relevant articles and documents

Indium-mediated allylation of carbonyl compounds in deep eutectic solvents

González-Gallardo, Nerea,Saavedra, Beatriz,Guillena, Gabriela,Ramón, Diego J.

, (2021/08/26)

This study describes, for the first time, the in situ generation of indium organometallic reagents in environmentally friendly deep eutectic solvents (DESs). The allylation process of different carbonyl compounds is achieved mediated by indium metal and u

A Mechanochemical Zinc-Mediated Barbier-Type Allylation Reaction under Ball-Milling Conditions

Yin, JieXiang,Stark, Roderick T.,Fallis, Ian A.,Browne, Duncan L.

, p. 2347 - 2354 (2020/02/04)

A ball-milling-enabled zinc-mediated Barbier-type allylation reaction is reported. Notably, running the reaction in this manner renders it effective irrespective of the initial morphology of the zinc metal. The process is operationally simple, does not re

Synthesis of Cyclopropanes via 1,3-migration of acyloxy groups triggered by formation of α-Imino Rhodium Carbenes

Xu, Ze-Feng,Liu, Jincheng,Chang, Xin,Chen, Tao,Xu, Huaping,Duan, Shengguo,Li, Chuan-Ying

supporting information, p. 5163 - 5169 (2020/07/16)

A novel and highly efficient synthetic approach to cyclopropanes was realized via 1,3-migration of acyloxy groups triggered by α-imino rhodium carbenes. Excellent chemoselectivity ensured broad compatibility of common functional groups. Merits such as readily available substrates, mild reaction conditions, and time-saving processes qualified this transformation as an attractive alternative strategy to synthesize multifunctionalized cyclopropanes. Primary investigations and discussion on the mechanism are presented.

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