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18232-70-7

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18232-70-7 Usage

General Description

Acetamide, 2-(4-chlorophenoxy)-N-methoxy-N-methyl- is a chemical compound that contains an acetamide group, a 4-chlorophenoxy group, a methoxy group, and a methyl group. Acetamide, 2-(4-chlorophenoxy)-N-methoxy-N-methyl- is commonly used as a herbicide due to its ability to control various types of weeds. It works by inhibiting plant growth enzymes, ultimately leading to the death of unwanted plants. Additionally, it may have potential applications in the pharmaceutical industry as a building block for the synthesis of other complex compounds. However, it is important to handle this chemical with caution as it may pose risks to human health and the environment if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 18232-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18232-70:
(7*1)+(6*8)+(5*2)+(4*3)+(3*2)+(2*7)+(1*0)=97
97 % 10 = 7
So 18232-70-7 is a valid CAS Registry Number.

18232-70-7SDS

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-chlorophenoxy)-N-methoxy-N-methylacetamide

1.2 Other means of identification

Product number -
Other names -

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:18232-70-7 SDS

18232-70-7Relevant articles and documents

Expedient synthesis of 3-alkoxymethyl- And 3-aminomethyl-pyrazolo[3,4-b] pyridines

Beutner, Gregory L.,Kuethe, Jeffrey T.,Kim, Mary M.,Yasuda, Nobuyoshi

supporting information; experimental part, p. 789 - 794 (2009/06/20)

An effective strategy has been developed for the preparation of 3-alkoxymethyl-pyrazolo[3,4-b]pyridines, compounds that are currently not readily accessible by existing synthetic methods. Further manipulation of these compounds allows for access to 3-alkoxymethyl-pyrazolo[3,4-b]pyridines with a variety of substitution patterns as well as 3-aminomethyl-pyrazolo[3,4-b] pyridines.

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