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2-chloro-2-methylpropanamide is an organic compound with the chemical formula C4H8ClNO. It is a derivative of propanamide, featuring a chloromethyl group (-CHCl) and a methyl group (-CH3) attached to the same carbon atom. 2-chloro-2-methylpropanamide is a colorless liquid with a pungent odor and is soluble in water and most organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle 2-chloro-2-methylpropanamide with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

7462-75-1

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7462-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7462-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7462-75:
(6*7)+(5*4)+(4*6)+(3*2)+(2*7)+(1*5)=111
111 % 10 = 1
So 7462-75-1 is a valid CAS Registry Number.

7462-75-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-2-methylpropanamide

1.2 Other means of identification

Product number -
Other names dimethylcarbamylmethyl 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:7462-75-1 SDS

7462-75-1Relevant academic research and scientific papers

Asymmetric auto-tandem catalysis with a planar-chiral ruthenium complex: Sequential allylic amidation and atom-transfer radical cyclization

Kanbayashi, Naoya,Takenaka, Kazuhiro,Okamura, Taka-Aki,Onitsuka, Kiyotaka

supporting information, p. 4897 - 4901 (2013/06/05)

Ru does it all: A novel example of an asymmetric auto-tandem reaction catalyzed by a planar-chiral cyclopentadienyl-ruthenium complex is described. The reaction of allylic chloride with α-haloamides provides synthetically useful, diastereomerically and enantiomerically enriched γ-lactams with multiple stereogenic centers through one-pot sequential allylic amidation/atom-transfer radical cyclization. PG=protecting group. Copyright

Chloropyridylcarbonyl derivatives

-

, (2008/06/13)

Novel chloropyridylcarbonyl derivatives of the formula STR1 in which Het is STR2 n is 1 or 2, R1 is hydrogen, optionally substituted C1-6 alkyl, optionally substituted C2-6 alkenyl, optionally substituted C3-6 alkynyl, optionally substituted phenyl or optionally substituted pyrimidinyl, and R2 and R3, independently of each other, are hydrogen or C1-4 alkyl, and acid addition salts and metal salt complexes thereof, are outstandingly active as microbicides.

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