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475060-42-5

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475060-42-5 Usage

General Description

Piperidine-3-carboxylic acid methyl amide hydrochloride is a chemical compound that belongs to the class of organic compounds known as dicarboximides. This chemical is known for its involvement in biological systems and its application in pharmaceuticals, particularly in the development of drugs. It possesses a variety of functional groups such as a carboxylic acid, an amide and a piperidine ring, contributing to its reactivity. It also contains a hydrochloride moiety, implying its acidic nature and solubility in water. Its well-defined chemical structure facilitates its precise use in various chemical reactions and laboratory procedures, contributing to its significance in research and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 475060-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,0,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 475060-42:
(8*4)+(7*7)+(6*5)+(5*0)+(4*6)+(3*0)+(2*4)+(1*2)=145
145 % 10 = 5
So 475060-42-5 is a valid CAS Registry Number.

475060-42-5Downstream Products

475060-42-5Relevant articles and documents

PHARMACEUTICAL COMPOUNDS

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Page/Page column 73-74, (2008/06/13)

Fused pyrimidines of formula (I); wherein A represents a thiophene or furan ring; n is 1 or 2; R1 is a group of formula (II); wherein m is 0 or 1; R30 is H or C1-C6 alkyl; R4 and R5 form, together with the N atom to which they are attached, a 5- or 6-membered saturated N-containing heterocyclic group which includes 0 or 1 additional heteroatoms selected from N, S and O, which may be fused to a benzene ring and which is unsubstituted or substituted; or one of R4 and R5 is alkyl and the other is a 5- or 6-membered saturated N-containing heterocyclic group as defined above or an alkyl group which is substituted by a 5- or 6-membered saturated N-containing heterocyclic group as defined above; R2 is selected from formula (a); wherein R6 and R7 form, together with the nitrogen atom to which they are attached, a morpholine, thiomorpholine, piperidine, piperazine, oxazepane or thiazepane group which is unsubstituted or substituted; and formula (b); wherein Y is a C2-C4 alkylene chain which contains, between constituent carbon atoms of the chain and/or at one or both ends of the chain, 1 or 2 heteroatoms selected from O, N and S, and which is unsubstituted or substituted; and R3 is an indazole group which is unsubstituted or substituted; and the pharmaceutically acceptable salt thereof have activity as inhibitors of P13K and may thus be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour associated with P13 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

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