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24486-64-4

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24486-64-4 Usage

General Description

2,4,6-tris(4-bromophenoxy)-1,3,5-triazine is a chemical compound consisting of a triazine ring with three 4-bromophenoxy substituents. It is commonly used as a herbicide, particularly for controlling broadleaf weeds in agricultural crops. 2,4,6-tris(4-bromophenoxy)-1,3,5-triazine works by inhibiting the photosynthetic electron transport in plants, disrupting their ability to produce energy from sunlight and ultimately leading to their death. Due to its potential environmental and health hazards, it is important to handle and use this chemical with caution and follow safety regulations and guidelines. Additionally, its persistence in the environment and potential toxicity to aquatic organisms also raise concerns about its impact on ecosystems.

Check Digit Verification of cas no

The CAS Registry Mumber 24486-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24486-64:
(7*2)+(6*4)+(5*4)+(4*8)+(3*6)+(2*6)+(1*4)=124
124 % 10 = 4
So 24486-64-4 is a valid CAS Registry Number.

24486-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tris(p-bromophenoxy)-1,3,5-triazine

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2,4,6-tris(phenylmethoxy)

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:24486-64-4 SDS

24486-64-4Relevant articles and documents

Nickel-catalysed C–O bond reduction of 2,4,6-triaryloxy-1,3,5-triazines in 2-methyltetrahydrofuran

Wang, Yaoyao,Shen, Jun,Chen, Qun,Wang, Liang,He, Mingyang

, p. 409 - 412 (2018/10/02)

A nickel-catalysed reduction of phenol derivatives activated by 2,4,6-trichloro-1,3,5-triazine (TCT) in ecofriendly 2-methyltetrahydrofuran (2-MeTHF) is described. The phenol-TCT derivatives were readily prepared using grinding method in short time without further purification. This catalytic system allowed the facile C–O cleavage of phenol-TCT derivatives under mild reaction conditions with high efficiency and good functional group tolerance. Gram-scale reaction was also achieved. Particularly, sequential functionalization of phenol-TCT derivatives followed by C–O bond reduction could also be realized, affording the high value-added products in moderate to good yields.

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