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51241-39-5

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51241-39-5 Usage

General Description

1-chloro-2-(pentyloxy)benzene is an organic chemical compound with both chloro and pentyloxy groups attached to a benzene ring. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 1-chloro-2-(pentyloxy)benzene is also known to have moderate toxicity and should be handled with care. It is important to follow proper safety protocols when working with 1-chloro-2-(pentyloxy)benzene to minimize the risk of exposure and adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 51241-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,4 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51241-39:
(7*5)+(6*1)+(5*2)+(4*4)+(3*1)+(2*3)+(1*9)=85
85 % 10 = 5
So 51241-39-5 is a valid CAS Registry Number.

51241-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-pentoxybenzene

1.2 Other means of identification

Product number -
Other names (2-Chlor-phenyl)-pentyl-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:51241-39-5 SDS

51241-39-5Relevant articles and documents

Regioselective Para Chlorination of Alkoxybenzenes by Use of Alumina Supported Copper(II) Chloride

Kodomari, Mitsuo,Takahashi, Shin,Yoshitomi, Suehiko

, p. 1901 - 1902 (1987)

Alkoxybenzenes were highly regioselectively chlorinated by use of copper(II) chloride supported on neutral alumina in chlorobenzene to give p-alkoxychlorobenzenes in high yield.The p/o ratios were more than 30.

SELECTIVITY OF AROMATIC CHLORINATION REACTIONS WITHIN A REVERSED-PHASE LIQUID CHROMATOGRAPHY COLUMN

Jaeger, David A.,Clennan, Malgorzata Wegrzyn,Leyden, Donald E.,Murthy, R. S. Shreedhara

, p. 4805 - 4808 (2007/10/02)

Substrate selectivity was obtained in the chlorination of a series of n-alkyl phenyl ethers by chlorine water on a reversed-phase high performance liquid chromatography column at 25 deg C.

POLY(ETHYLENE GLYCOL)S AS PHASE TRANSFER CATALYSTS IN THE ALKOXYLATION OF HALOBENZENES OF ALKYL ARYL ETHERS

Neumann, R.,Sasson, Y.

, p. 3437 - 3440 (2007/10/02)

Mono and di-halobenzenes and alkoxide ions gave monoalkoxybenzenes, but no phenols, when catalyzed by high molecular weight poly(ethylene glycol)s as phase transfer catalysts.Bromobenzenes were more reactive than chlorobenzenes but gave more side products, and for alcohols the reactivity was primary>secondary>tertiary.

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