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16738-07-1

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16738-07-1 Usage

General Description

(2,4-dibromophenoxy)acetyl chloride is a chemical compound with the molecular formula C8H6Br2ClO3. It is a derivative of acetyl chloride, with two bromine atoms attached to a phenoxy group. (2,4-dibromophenoxy)acetyl chloride is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is a versatile reagent that is used in the synthesis of a wide range of organic compounds, and its reactivity makes it a valuable tool in the field of chemical research. Additionally, it is important to handle (2,4-dibromophenoxy)acetyl chloride with caution, as it is highly reactive and can cause skin and eye irritation upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 16738-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,3 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16738-07:
(7*1)+(6*6)+(5*7)+(4*3)+(3*8)+(2*0)+(1*7)=121
121 % 10 = 1
So 16738-07-1 is a valid CAS Registry Number.

16738-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dibromophenoxy)acetyl chloride

1.2 Other means of identification

Product number -
Other names (2,4-DIBROMOPHENOXY)ACETYL CHLORIDE

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:16738-07-1 SDS

16738-07-1Relevant articles and documents

Studies of O,O-Dimethyl α-(2,4-Dichlorophenoxyacetoxy) ethylphosphonate (HW02) as a new herbicide. 1. Synthesis and herbicidal activity of HW02 and analogues as novel inhibitors of pyruvate dehydrogenase complex

He, Hong-Wu,Yuan, Jun-Lin,Peng, Hao,Chen, Ting,Shen, Ping,Wan, Shu-Qing,Lee, Yanjun,Tan, Hong-Liang,He, Ya-Hui,He, Jun-Bo,Li, Yan

, p. 4801 - 4813 (2011/12/04)

On the basis of the previous work for optimization of O,O-diethyl α-(substituted phenoxyacetoxy)alkylphosphonates, further extensive syntheticmodifications were made to the substituents in alkylphosphonate and phenoxymoieties of the title compounds. New O,O-dimethyl α-(substituted phenoxyacetoxy)alkylphosphonates were synthesized as potential inhibitors of pyruvate dehydorogenase complex (PDHc). Their herbicidal activity and efficacy in vitro against PDHc were examined. Some of these compounds exhibited significant herbicidal activity and were demonstrated to be effective inhibitors of PDHc from three different plants. The structure-activity relationships of these compounds including previously reported analogous compoundswere studied by examining their herbicidal activities. Both inhibitory potency against PDHc and herbicidal activity of title compounds could be increased greatly by optimizing substituent groups of the title compounds. O,O-Dimethyl α-(2,4- dichlorophenoxyacetoxy)ethylphosphonate (I-5), which acted as a competitive inhibitor of PDHc with much higher inhibitory potency against PDHc from Pisum sativum and Phaseolus radiatus than from Oryza sativa, was found to be themost effective compound against broadleaf weeds and showed potential utility as herbicide.

Synthesis and Antimicrobial Activity of N-piperazines/morpholines

Chaurasia, Sunita,Srivastava, Savitri D.

, p. 45 - 46 (2007/10/02)

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Synthesis and biological evaluation of some novel N-2-(phenoxy/bromo/nitro/methyl/naphtoxy and substituted-phenoxy)-acetylphenothiazine

Chaurasia,Srivastava

, p. 106 - 107 (2007/10/02)

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