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1-Piperidinecarboxylic acid, 4-[5-methyl-4-(phenylmethyl)-4H-1,2,4-triazol-3-yl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

685827-98-9

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685827-98-9 Usage

Molecular weight

348.43 g/mol This is the mass of one mole of the compound, calculated from its molecular formula.

Biological and pharmaceutical significance

Used as a precursor in the synthesis of various pharmaceutical drugs 1-Piperidinecarboxylic acid, 4-[5-methyl-4-(phenylmethyl)-4H-1,2,4-triazol-3-yl]-, 1,1-dimethylethyl ester serves as a starting material for creating other drugs with antifungal and antimicrobial properties.

Potential drug candidate

Therapeutic applications due to enzyme and protein inhibition The compound has the potential to be developed into a drug because of its ability to inhibit certain enzymes and proteins in the body, which may have therapeutic benefits.

Research and development

New drugs for the treatment of various diseases and medical conditions The compound is used in the research and development of new drugs to treat a range of diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 685827-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,8,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 685827-98:
(8*6)+(7*8)+(6*5)+(5*8)+(4*2)+(3*7)+(2*9)+(1*8)=229
229 % 10 = 9
So 685827-98-9 is a valid CAS Registry Number.

685827-98-9Relevant academic research and scientific papers

TRIAZOLE COMPOUNDS FOR THE TREATMENT OF DYSMENORRHOEA

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Page 41, (2010/02/06)

A compound of formula (I), a pharmaceutically acceptable salt or solvate thereof, wherein R' represents C,-C6 alkyl,-(CH2)c-[C3-C8 cycloalkyl]-,-(CH2)C-W or-(CH2)C-Z-(CH2)dW; W represents C1-C6 alkyl, C1-C6 alkyloxy,-C02[C1-C6 alkyl],-CONR4R5, an optionally substituted phenyl group, NR4R5, het2 or het3; Z represents O or S(O)g; g represents 0, 1 or 2; R2 represents a phenyl group, optionally fused to a 5-or 6-membered aryl or heterocyclic group which may contain one or more heteroatoms selected from N, O or S; the phenyl group and the optionally fused group being optionally substituted; Ring A represents a 4-, 5-or 6-membered saturated heterocyclic group containing at least one N; Ring B represents a phenyl group or het1, each group being optionally substituted; R7 independently represents H1 C1-C6alkyl, OR3,-(CH2)e-R3 or-(CH2)f-O-(CH2)e-R3; at each occurrence R3 independently represents H1 C1-C6 alkyl optionally substituted by Y,-(CH2)g [C3-C8 cycloalkyl], phenyl, benzyl, pyridyl or pyrimidyl; at each occurrence R4 and R5independently represent H1 Cl-C6 alkyl (optionally substituted with Cl-C6alkyloxy), (CH2)gC02-[C1-C6 alkyl],-S02Me,-(CH2)g[C3-C8 cycloalkyl], S02Me, phenyl, benzyl, pyridyl or pyrimidyl; or R4 and R5 together with the N atom to which they are attached represent a heterocyclic group of from 3 to 8 atoms; Y independently represents a phenyl group, NR4R5 or het4, the phenyl group being optionally substituted; het1 represents a 4-, 5-or 6-membered saturated, or unsaturated, heterocyclic group containing at least one N (but which may also contain one or more O or S atoms); het2 and het4 represent an optionally substituted 4-, 5-, 6-or 7-membered saturated, or unsaturated, heterocyclic group containing at least one N (but which may 5 also contain one or more O or S atoms); het3 represents an optionally substituted 4-, 5-, 6-or 7-membered saturated, or unsaturated, heterocyclic group containing at least one O (but which may also contain one or mare N or S atoms); at each occurrence R6 independently represents H1 C1-C6 alkyl optionally substituted by Y, =(CH2)g [C3-C8 cycloalkyl], phenyl, benzyl, pyridyl or pyrimidyl; a and b independently represent 0 or 1; c,, d, a end g independently represent 0, 1, 2, 3 or 4; . f índeperldently represents 1, 2, 3 or 4; provided that: (i) a + b cannot equal 0; and províded,that,when R1 represents-(CH2)c-Z-(CH2)d-W and W represents.NR4R5 or any N linked heterocyclic, group then d must not be, 0 or 1; and (iii), provided that when R2 represents a phenyl group substituted by a group of, formula-(CH2)eOR3,-(CH2)e-OCOR3 or-(CH2)e,OCOR3 ;or het1,and/or het2 are substituted by a group of formula-(CH2)eOR3, (CH2),-CO2R3 or-(CH2)eOCOR3; or when R7 represents-OR3 or-(CH2)f-0-(CH2)e-R3 and e is 0; or when W represents a phenyl group substituted with-OR3 or-C02R3 and R3 represents an alkyl group substituted with Y, and Y represents NR4R5 or an N-Finked het3; then, R3, must,represent,C2-C6 alkyl substituted with. Y. are useful in the treatment of dysmenorrhoea.

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