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186805-79-8

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186805-79-8 Usage

General Description

2,6-dichloro-4-hydroxy-1-benzyloxybenzene is a chemical compound with the molecular formula C13H10Cl2O2. It is a derivative of benzene with two chlorine atoms and a hydroxyl group attached to the 2 and 4 positions, respectively. Additionally, it has a benzyloxy group attached to the 1 position. 2,6-dichloro-4-hydroxy-1-benzyloxybenzene is commonly used in organic synthesis as an intermediate for the production of pharmaceuticals, agrochemicals, and dyes. It is also known for its potential antioxidant and anti-inflammatory properties, making it of interest for medicinal and cosmetic applications. Due to its molecular structure and properties, precautions must be taken when handling and storing this chemical to avoid potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 186805-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,8,0 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 186805-79:
(8*1)+(7*8)+(6*6)+(5*8)+(4*0)+(3*5)+(2*7)+(1*9)=178
178 % 10 = 8
So 186805-79-8 is a valid CAS Registry Number.

186805-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-hydroxy-1-benzyloxybenzene

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:186805-79-8 SDS

186805-79-8Relevant articles and documents

First total syntheses of cytotoxic substances russuphelins A-C

Reddy, K. Laxma,Vittal

, p. 107 - 118 (2007/10/03)

Russuphelins (A-C) are synthesized from 2,4,6-trichlorophenol, using Michael type nucleophilic displacement of halides on 2,6-dihaloquinone followed by simple chemical manipulations.

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