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18113-14-9

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18113-14-9 Usage

Usage

Found in personal care products like soaps, toothpaste, and deodorants

Antimicrobial Properties

Strong antibacterial and antifungal effects
Effective against a broad spectrum of microorganisms

Concerns

Human Health:
Linked to hormone disruption
Associated with antibiotic resistance
Environmental Impact:
Causes environmental contamination

Regulatory Status

Restricted or banned in certain products by some countries and organizations

Research

Ongoing studies to understand associated risks
Efforts to develop alternative antimicrobial compounds

Check Digit Verification of cas no

The CAS Registry Mumber 18113-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,1 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18113-14:
(7*1)+(6*8)+(5*1)+(4*1)+(3*3)+(2*1)+(1*4)=79
79 % 10 = 9
So 18113-14-9 is a valid CAS Registry Number.

18113-14-9SDS

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 2,5-dichloro-4-methoxyphenol

1.2 Other means of identification

Product number -
Other names hydroxy demosan

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:18113-14-9 SDS

18113-14-9Relevant articles and documents

Synthesis of o-chlorophenols via an unexpected nucleophilic chlorination of quinone monoketals mediated by N,N′-dimethylhydrazine dihydrochloride

Yin, Zhiwei,Zhang, Jinzhu,Wu, Jing,Green, Riana,Li, Sihan,Zheng, Shengping

, p. 2854 - 2858 (2014/05/06)

An unexpected nucleophilic chlorination of a quinone monoketal while carrying out a pyrazolidine synthesis has led to a general preparation of multisubstituted phenols. The products are obtained in good to high yields under mild conditions. The bridged pyrazolidines that were the original targets are obtained in the presence of a protic solvent. This journal is the Partner Organisations 2014.

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