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2-(2-chloroethyl)-1,4-dimethoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51016-50-3

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51016-50-3 Usage

Chemical family

Phenols (aromatic ring with hydroxyl group attached)

Substituents

Two methoxy groups and a chloroethyl group attached to the benzene ring

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Potential use

Treatment of cancer (inhibits certain enzymes involved in cell growth)

Hazard classification

Hazardous chemical

Health effects

Skin and eye irritation, respiratory and central nervous system effects (if inhaled or ingested)

Check Digit Verification of cas no

The CAS Registry Mumber 51016-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,1 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51016-50:
(7*5)+(6*1)+(5*0)+(4*1)+(3*6)+(2*5)+(1*0)=73
73 % 10 = 3
So 51016-50-3 is a valid CAS Registry Number.

51016-50-3SDS

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 2-(2-chloroethyl)-1,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 2-(2-Chlor-aethyl)-1,4-dimethoxy-benzol

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:51016-50-3 SDS

51016-50-3Relevant academic research and scientific papers

SYNTHESIS AND SOME PROPERTIES OF 1,2-DIHYDRO-4,7-DIHYDROXYCYCLOBUTANAPHTHALENE-3,8-DIONE AND 1,2,5,6-TETRAHYDRO-4,7-DIHYDROXYDICYCLOBUTANAPHTHALENE-3,8-DIONE

Watabe, Takashi,Oda, Masaji

, p. 1791 - 1794 (2007/10/02)

Title compounds have been first synthesized.The effects of strain due to the cyclobutene annelation are observed in the 13C NMR chemical shifts, tautomeric equilibrium, reduction potentials, and Diels-Alder reactions with dienes; thermolytic Diels-Alder reactions with dienophiles give novel polycyclic hydroxyquinones.

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