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23003-29-4

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23003-29-4 Usage

General Description

2,4-Dibromo-3-hydroxy-6-picoline, also known as bromoxynil, is a synthetic compound that is commonly used as an herbicide to control broadleaf weeds in crops such as cereals, cotton, and vegetables. It works by blocking the essential enzyme system in plants, ultimately leading to their death. Bromoxynil is a highly effective and fast-acting herbicide, with low toxicity to mammals, birds, and aquatic organisms. However, it can be toxic to some non-target plants and may have some negative impacts on the environment. Therefore, it is important to use this chemical with caution and follow recommended application guidelines to minimize potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 23003-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,0 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23003-29:
(7*2)+(6*3)+(5*0)+(4*0)+(3*3)+(2*2)+(1*9)=54
54 % 10 = 4
So 23003-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H5Br2NO/c1-3-2-4(7)5(10)6(8)9-3/h2,10H,1H3

23003-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromo-6-methylpyridin-3-ol

1.2 Other means of identification

Product number -
Other names 2,4-Dibromo-3-hydroxy-6-picoline

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:23003-29-4 SDS

23003-29-4Upstream product

23003-29-4Relevant articles and documents

Efficient regioselective preparation of monobromo and bromoiodo hydroxy pyridines from dibromoderivatives via bromine-lithium exchange

Meana, ángela,Rodríguez, Justo F.,Sanz-Tejedor, M. Ascensión,García-Ruano, José L.

, p. 1678 - 1682 (2007/10/03)

Annular dibromination of hydroxypyridines with NBS in acetonitrile followed by bromine-lithium exchange with RLi and subsequent trapping with H2O or I2 afforded monobromo and bromoiodo derivatives in a completely regioselective way. Iodination of bromo hydroxypyridines with NIS is totally regioselective.

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