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32111-91-4

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32111-91-4 Usage

General Description

(4-chlorophenyl)methylcyanamide, also known as chlorphenamide, is a chemical compound with the formula C8H8ClN3. It is an organic compound that is commonly used in the pharmaceutical industry as a carbonic anhydrase inhibitor, which means it can help to reduce the production of fluids in the body, such as cerebrospinal fluid and aqueous humor. This makes it a useful medication for treating conditions such as glaucoma, epilepsy, and edema. As a cyanamide derivative, it is also used as a building block in the synthesis of other organic and pharmaceutical compounds. However, it is important to note that chlorphenamide is a toxic and potentially hazardous substance, so it should be handled with care and used only by qualified professionals.

Check Digit Verification of cas no

The CAS Registry Mumber 32111-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32111-91:
(7*3)+(6*2)+(5*1)+(4*1)+(3*1)+(2*9)+(1*1)=64
64 % 10 = 4
So 32111-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2/c9-8-3-1-7(2-4-8)5-11-6-10/h1-4,11H,5H2

32111-91-4Relevant articles and documents

N-(4-Chlorophenyl)-N-methylcyanamide

Cunningham, Ian D.,Light, Mark E.,Hursthouse, Michael B.

, p. 1833 - 1835 (1999)

An X-ray structural analysis of the title compound, C8H7ClN2, shows an essentially planar molecule, but with an unusually long aryl-C to planar-N bond.

ARYLAZOMETHYLENETRIPHENYLPHOSPHORANES: A STUDY OF THE ALKYLATION REACTION

Alemagna, Andreina,Buttero, Paolo Del,Licandro, Emanuela,Papagni, Antonio

, p. 249 - 252 (2007/10/02)

The title compounds undergo alkylation reaction at the nitrogen β to the ylidic carbon atom: the nature of the reaction products depends on the alkylating reagent and on the nature of the solvent.

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