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24967-79-1

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24967-79-1 Usage

Molecular Weight

330.80 g/mol

Structure

Three bromine atoms (tri-bromo) attached to positions 2, 4, and 6 of the phenol ring
One methoxy group (-OCH3) attached to position 3 of the phenol ring

Usage

Flame Retardant: Commonly employed to reduce flammability in various materials such as plastics, textiles, and electronics.
Preservative: Used in some personal care products for its preservative properties.
Intermediate: Serves as an intermediate compound in the synthesis of other organic compounds.

Toxicity

Considered toxic, posing potential health risks.

Environmental Concerns

Due to its toxicity and potential environmental impact, there is growing scrutiny of its usage.

Regulatory Attention

Ongoing efforts to develop safer alternatives to address health and environmental concerns associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 24967-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24967-79:
(7*2)+(6*4)+(5*9)+(4*6)+(3*7)+(2*7)+(1*9)=151
151 % 10 = 1
So 24967-79-1 is a valid CAS Registry Number.

24967-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIBROMO-3-METHOXYPHENOL

1.2 Other means of identification

Product number -
Other names 2,4,6-Tribrom-3-methoxy-phenol

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:24967-79-1 SDS

24967-79-1Relevant articles and documents

-

Kohn

, p. 1601 (1952)

-

Pyridinium hydrobromide perbromide induces ipsobromodeformylation in o-hydroxy and o-methoxy substituted aromatic aldehydes

Córdoba, Rubén,Plumet, Joaquín

, p. 9303 - 9305 (2007/10/03)

The reaction of o-hydroxy and o-methoxy substituted aromatic aldehydes with PHPB in pyridine gives aromatic bromination products including those arising from ipsobromodeformylation.

Bromination of Phenols by Use of Benzyltrimethylammonium Tribromide

Kajigaeshi, Shoji,Kakinami, Takaaki,Tokiyama, Hajime,Hirakawa, Takahiro,Okamoto, Tsuyoshi

, p. 627 - 630 (2007/10/02)

The reaction of phenols with benzyltrimethylammonium tribromide in dichloromethane-methanol for 1 h at room temperature gave polybromophenols in good yields.

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