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7399-57-7

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7399-57-7 Usage

Derivative of acetamide

The compound is derived from acetamide, which is a common functional group in organic chemistry.

Chloro and methyl group attached to a phenoxy ring

The compound contains a chlorine atom and a methyl group attached to a phenoxy ring, which is a benzene ring with an ether functional group.

Widely used as a herbicide

The compound is commonly used to control broadleaf weeds in agricultural crops.

Inhibits the growth of target plants

The herbicide works by disrupting the synthesis of fatty acids in target plants, ultimately leading to their death.

Can be harmful if ingested or inhaled

The chemical can cause harm to humans if ingested or inhaled.

Can cause skin and eye irritation

The compound may cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 7399-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7399-57:
(6*7)+(5*3)+(4*9)+(3*9)+(2*5)+(1*7)=137
137 % 10 = 7
So 7399-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10ClNO2/c1-6-4-7(10)2-3-8(6)13-5-9(11)12/h2-4H,5H2,1H3,(H2,11,12)

7399-57-7SDS

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-(4-chloro-2-methylphenoxy)acetamide

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-chlor-phenoxyessigsaeureamid

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:7399-57-7 SDS

7399-57-7Relevant articles and documents

Visible light-mediated synthesis of amides from carboxylic acids and amine-boranes

Chen, Xuenian,Kang, Jia-Xin,Ma, Yan-Na,Miao, Yu-Qi

supporting information, p. 3595 - 3599 (2021/06/06)

Here, a photocatalytic deoxygenative amidation protocol using readily available amine-boranes and carboxylic acids is described. This approach features mild conditions, moderate-to-good yields, easy scale-up, and up to 62 examples of functionalized amides with diverse substituents. The synthetic robustness of this method was also demonstrated by its application in the late-stage functionalization of several pharmaceutical molecules.

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