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2-(3-bromopropoxy)-4-methyl-1-(propan-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26646-40-2

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26646-40-2 Usage

Molecular structure

A complex organic molecule with a benzene ring, a methyl group, an isopropyl group, and a bromopropoxy group attached.

Functional groups

Bromopropoxy, methyl, and isopropyl groups.

Molecular weight

267.21 g/mol.

Usage

Commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

Applications

Fields of organic chemistry, drug discovery, new materials development, and industrial processes.

Safety precautions

Handle and store with appropriate safety measures due to chemical reactivity and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 26646-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,4 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26646-40:
(7*2)+(6*6)+(5*6)+(4*4)+(3*6)+(2*4)+(1*0)=122
122 % 10 = 2
So 26646-40-2 is a valid CAS Registry Number.

26646-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-bromopropoxy)-4-methyl-1-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names (3-Brom-propyl)-(2-isopropyl-5-methyl-phenyl)-aether

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:26646-40-2 SDS

26646-40-2Relevant academic research and scientific papers

Synthesis of N-aryloxyalkylanabasine derivatives

Slyn'Ko,Tatarova,Shakirov,Shul'Ts

, p. 294 - 301 (2013/07/26)

N-Aryloxyalkylanabasine derivatives were prepared via the reaction of anabasine hydrochloride with various aryloxyhaloalkanes in the presence of potash in DMF. The reaction occurred with retention of the chiral center C-(2) of the piperidine group. Side products of bis(aryloxy)ethanes were characterized.

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