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6641-02-7

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6641-02-7 Usage

General Description

2,4-Dichloro-6-(hydroxymethyl)phenol, also known as triclosan, is a synthetic chemical with antimicrobial properties that is commonly used in personal care products, household goods, and medical supplies. It works by disrupting the cell membranes of bacteria and other microorganisms, effectively killing them. However, concerns have been raised about its potential contribution to antibiotic resistance and negative impacts on human health and the environment. Triclosan has been linked to hormone disruption, development of resistant bacteria, and environmental contamination. Due to these concerns, its use in consumer products has been restricted in some countries, and alternatives are being sought.

Check Digit Verification of cas no

The CAS Registry Mumber 6641-02-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6641-02:
(6*6)+(5*6)+(4*4)+(3*1)+(2*0)+(1*2)=87
87 % 10 = 7
So 6641-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2O2/c8-5-1-4(3-10)7(11)6(9)2-5/h1-2,10-11H,3H2

6641-02-7SDS

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 2,4-DICHLORO-6-(HYDROXYMETHYL)PHENOL

1.2 Other means of identification

Product number -
Other names 3,5-Dichlor-2-hydroxy-benzylalkohol

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:6641-02-7 SDS

6641-02-7Relevant articles and documents

Asymmetric Retro-Claisen Reaction by Synergistic Chiral Primary Amine/Palladium Catalysis

Han, Yanfang,Zhang, Long,Luo, Sanzhong

supporting information, p. 7258 - 7261 (2019/10/02)

We described herein a chiral primary amine/palladium catalyzed asymmetric retro-Claisen reaction of β-diketones with salicylic carbonates. A series of chiral α-alkylated ketones and macrolides were obtained with good yields and excellent enantioselectivities upon a sequence of decarboxylative benzylation, retro-Claisen cleavage, and enamine protonation. This strategy features broad substrate scope, mild conditions, as well as high atom economy with salicylic carbonates as the o-quinone methide precursors.

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