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1-(3-Methylphenyl)cyclopropanemethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

886366-44-5

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886366-44-5 Usage

Structure

Cyclopropane derivative with a hydroxyl group attached to a cyclopropane ring and a methylphenyl group

Application

Used in organic chemistry as a building block for the synthesis of various pharmaceuticals and bioactive compounds

Usage

Employed in the synthesis of organic materials and as a reagent in chemical research

Significance

Unique structure and reactivity make it a valuable intermediate for the production of diverse chemical compounds

Check Digit Verification of cas no

The CAS Registry Mumber 886366-44-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 886366-44:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*6)+(2*4)+(1*4)=225
225 % 10 = 5
So 886366-44-5 is a valid CAS Registry Number.

886366-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(3-methylphenyl)cyclopropyl]methanol

1.2 Other means of identification

Product number -
Other names CYCLOPROPANEMETHANOL,1-(3-METHYLPHENYL)

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:886366-44-5 SDS

886366-44-5Downstream Products

886366-44-5Relevant academic research and scientific papers

Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds

Lee, Taegyo,Hartwig, John F.

, p. 8723 - 8727 (2016/07/21)

Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of

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