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2415-96-5

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2415-96-5 Usage

General Description

2,2,3,3-Tetramethylcyclopropanemethanol is a chemical compound with the molecular formula C9H18O. It is a cyclic alcohol with a four-membered cyclopropane ring and four methyl groups attached to the carbon atoms. 2,2,3,3-Tetramethylcyclopropanemethanol is used as a building block in organic synthesis and can be used to prepare various other organic compounds. It is also used as a solvent in some industries. The chemical properties and reactivity of 2,2,3,3-Tetramethylcyclopropanemethanol make it a versatile and valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 2415-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2415-96:
(6*2)+(5*4)+(4*1)+(3*5)+(2*9)+(1*6)=75
75 % 10 = 5
So 2415-96-5 is a valid CAS Registry Number.

2415-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2,3,3-tetramethylcyclopropyl)methanol

1.2 Other means of identification

Product number -
Other names 2,2,3,3-Tetramethylcyclopropanemethanol

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:2415-96-5 SDS

2415-96-5Relevant articles and documents

Cyclopropanation of allylic alcohols using substituted haloalkylzinc reagents: Synthesis of gem-Dimethylcyclopropanes

Charette,Wilb

, p. 176 - 178 (2007/10/03)

gem-Dimethylcyclopropanes were obtained by a cyclopropanation of allylic alcohols and ethers using a mixture of diethylzinc and 2,2-diiodopropane in 53-96% yields. Enantioenriched gem-dimethylcyclopropanes were also synthesized using a glucose-derived aux

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