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910032-21-2

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910032-21-2 Usage

Structure

Benzene derivative with a bromoethoxy group, a chloro group, and a methyl group

Physical state

Clear, colorless to pale yellow liquid

Solubility

Soluble in organic solvents

Odor

Characteristic odor

Usage

Used in various organic synthesis and chemical reactions as a starting material or intermediate

Primary applications

Manufacturing of pharmaceuticals, agrochemicals, and specialty chemicals

Safety precautions

Handle with care and follow proper safety procedures when working with it

Check Digit Verification of cas no

The CAS Registry Mumber 910032-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,0,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 910032-21:
(8*9)+(7*1)+(6*0)+(5*0)+(4*3)+(3*2)+(2*2)+(1*1)=102
102 % 10 = 2
So 910032-21-2 is a valid CAS Registry Number.

910032-21-2SDS

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-(2-bromoethoxy)-1-chloro-4-methylbenzene

1.2 Other means of identification

Product number -
Other names -

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:910032-21-2 SDS

910032-21-2Relevant articles and documents

Design, synthesis and anticonvulsant-analgesic activity of new N-[(phenoxy)alkyl]- and N-[(phenoxy)ethoxyethyl]aminoalkanols

Rapacz, Anna,Waszkielewicz, Anna M.,Pańczyk, Katarzyna,Pytka, Karolina,Koczurkiewicz, Paulina,Piska, Kamil,P?kala, El?bieta,Budziszewska, Bogus?awa,Starek-?wiechowicz, Beata,Marona, Henryk

, p. 220 - 238 (2017/02/05)

New derivatives of N-[(phenoxy)alkyl]- and N-[(phenoxy)ethoxyethyl]aminoalkanols have been synthesized and evaluated for their anticonvulsant activity in maximal electroshock (MES), maximal electroshock seizure threshold (MEST), and pentylenetetrazol (PTZ) tests. Their neurotoxicity was evaluated via rotarod and chimney tests. The compounds exhibiting the most beneficial activity and protection indices were evaluated for analgesic activity using the formalin test for neurogenic pain. They were also evaluated for their influence on cytotoxic activity using in vitro cellular models (HepG2 and CRL-2534 cell lines). Experiments performed using MTT and neutral red cytotoxicity assays showed that all evaluated compounds were safe for normal, glial cells (astrocytes) and did not induce hepatotoxic effects. Based on the results from the in vitro studies, the safety of the evaluated compounds was inferred. The most promising compound in this research was 1-{2-[2-(2,3-dimethylphenoxy)ethoxy]ethyl}piperidin-3-ol hydrochloride. Additionally, in silico metabolism prediction for the compound has been performed.

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