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alpha-cyclopropyl-4-methylbenzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6552-46-1

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6552-46-1 Usage

Chemical Classification

Cyclopropyl-containing alcohol

Structure

Cyclopropyl group attached to a 4-methylbenzyl moiety

Properties

Unique reactivity due to cyclopropyl group
Versatile building block in organic synthesis
Potential applications in drug development

Applications

Synthesis of organic compounds
Drug and pharmaceutical development

Interest in Research

Studying reactivity and behavior of cyclopropyl-containing compounds

Overall

Diverse potential uses and applications in scientific and industrial settings

Check Digit Verification of cas no

The CAS Registry Mumber 6552-46-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6552-46:
(6*6)+(5*5)+(4*5)+(3*2)+(2*4)+(1*6)=101
101 % 10 = 1
So 6552-46-1 is a valid CAS Registry Number.

6552-46-1SDS

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-methylphenylcyclopropylcarbinol

1.2 Other means of identification

Product number -
Other names Benzenemethanol, α-cyclopropyl-4-methyl-

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:6552-46-1 SDS

6552-46-1Relevant academic research and scientific papers

CuBr2-catalyzed ring opening/formylation reaction of cyclopropyl carbinols with DMF to synthesize formate esters

Zhuang, Daijiao,Gatera, Tharcisse,Yan, Rulong

supporting information, (2020/10/19)

An unprecedented protocol for the synthesis of formate esters has been developed by employing N,N-dimethylformamide (DMF) as both the source of CHO and solvent. This reaction undergoes ring opening of the cyclopropyl carbinols and in situ formation of homoallylic alcohols, which reacts with DMF to give the desired products. The substrate cyclopropyl carbinols with different groups participate smoothly in this process and the desired products are obtained in moderate to good yields.

A method for synthesis of homoallylic bromide

Qi, Wenke,Wang, Peipei,Fan, Liyuan,Zhang, Songlin

, p. 5918 - 5924 (2013/07/26)

Cyclopropyl Grignard reagents react with carbonyl compounds in the presence of diethyl phosphite to give homoallylic bromides. The reaction is effectively carried out under mild conditions in a one-pot fashion with moderate to good yields.

Regiospecific Nucleophilic Substitution in Cyclopropylcarbinols. Stereospecific Opening of the Cyclopropane Ring

Matveeva,Kvasha,Kurts

, p. 17 - 20 (2007/10/03)

Reactions of cyclopropylcarbinols with hydrobromic acid and the triphenylphosphine-tetrabromomethane complex at 0°C result in stereospecific opening of the cyclopropane ring with formation of trans-homoallyl bromides.

Mechanistic Evidence regarding the Magnesium Halide Transformation of Cyclopropylmethanols into Homoallylic Halides

McCormick, J. P.,Fitterman, Alan S.,Barton, Donald L.

, p. 4708 - 4712 (2007/10/02)

Cyclopropylmethanols are converted into homoallylic halides in high yield by treatment with magnesium bromide or iodide in refluxing, anhydrous diethyl ether.For uncovering of the details of the reaction mechanism, (cyclopropylphenylmethoxy)magnesium bromide (3a) was prepared by treatment of cyclopropylphenylmethanol (1) with hydridomagnesium bromide.Alkoyoxymagnesium bromide 3a was stable in refluxing diethyl ether and was not changed when treated with tetrabutylammonium bromide but was transformed into 4-bromo-1-phenyl-1-butene by treatment with hydrogen bromide or magnesium bromide.These results, together with first-order kinetics for the reaction of magnesium halide with 1, suggest a mechanism involving rapid formation of an intermediate ion pair (4), a magnesium oxonium bromide, which undergoes rate-determining ring opening to give homoallylic halide.A Hammett study of the reaction of substituted cyclopropylphenylmethanols with magnesium iodide provides a p value of -1.82, revealing substantial positive charge development on the carbinol carbon in the latter step.This investigation provides one of only a very few reported examples of Hammett studies used to probe positive charge development for a reaction carried out in anhydrous diethyl ether.

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