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"Acetamide, N-(chloromethyl)-N-methyl-" is a chemical compound with the molecular formula C4H8ClNO. It is a derivative of acetamide, where a methyl group and a chloromethyl group are attached to the nitrogen atom. Acetamide, N-(chloromethyl)-N-methyl- is also known as N-methyl-N-(chloromethyl)acetamide or Methyl chloromethyl acetamide. It is a colorless liquid with a pungent odor and is soluble in water. Due to its reactivity, it is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is important to handle Acetamide, N-(chloromethyl)-N-methyl- with care, as it can be harmful if inhaled, ingested, or absorbed through the skin, and it may cause irritation to the eyes, skin, and respiratory system.

4270-65-9

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4270-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4270-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4270-65:
(6*4)+(5*2)+(4*7)+(3*0)+(2*6)+(1*5)=79
79 % 10 = 9
So 4270-65-9 is a valid CAS Registry Number.

4270-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Chloromethyl-N-methylacetamide

1.2 Other means of identification

Product number -
Other names N-methyl-N-acetylaminomethyl 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:4270-65-9 SDS

4270-65-9Relevant academic research and scientific papers

Acyl Halide Induced Cleavage of N-Acylated Aminals

Boehme, Horst,Raude, Edgar

, p. 3421 - 3429 (2007/10/02)

Acyl halides attack N-acylated aminals 6 at the amine nitrogen as well as at the carboxamide group to form either N-halomethyl carboxamides 5 besides N,N-dialkyl carboxamides 11, or diacylamines 12 besides N,N-dialkylmethaneiminium halides 4.Depending on the variation of the substituents on both heteroatoms the cleavage may be directed to follow only one or the other pathway.Of highly synthetic interest is the broadly applicable preparation of methaneiminium salts 4 having bulky substituents on nitrogen by means of cleavage of the corresponding N,N-dialkyl-N'-formyl-N'-methylmethanediamines 6.

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