915296-81-0 Usage
Description
2-Chloromethyl-4-(2,4-dichlorophenyl)-6-methylpyridine-3,5-dicarboxylic acid 5-benzyl 3-ethyl ester is a complex organic chemical compound characterized by a pyridine ring with a chloromethyl group, a 2,4-dichlorophenyl group, and two carboxylic acid groups. It also features a benzyl group and an ethyl ester group, which contribute to its unique chemical properties and potential applications.
Used in Organic Chemistry:
2-Chloromethyl-4-(2,4-dichlorophenyl)-6-methylpyridine-3,5-dicarboxylic acid 5-benzyl 3-ethyl ester is used as a building block for the synthesis of other complex organic compounds due to its diverse functional groups and structural features.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloromethyl-4-(2,4-dichlorophenyl)-6-methylpyridine-3,5-dicarboxylic acid 5-benzyl 3-ethyl ester is used as an intermediate in the development of new drugs, potentially offering novel therapeutic properties and mechanisms of action.
Used in Agrochemicals:
2-Chloromethyl-4-(2,4-dichlorophenyl)-6-methylpyridine-3,5-dicarboxylic acid 5-benzyl 3-ethyl ester is used as a precursor in the production of agrochemicals, such as pesticides and herbicides, where its specific chemical properties may provide advantages in controlling agricultural pests and weeds.
Further research and experimentation are required to fully explore the potential uses and effects of 2-Chloromethyl-4-(2,4-dichlorophenyl)-6-methylpyridine-3,5-dicarboxylic acid 5-benzyl 3-ethyl ester in these industries and to determine its safety and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 915296-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,2,9 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 915296-81:
(8*9)+(7*1)+(6*5)+(5*2)+(4*9)+(3*6)+(2*8)+(1*1)=190
190 % 10 = 0
So 915296-81-0 is a valid CAS Registry Number.
InChI:InChI=1/C24H20Cl3NO4/c1-3-31-24(30)22-19(12-25)28-14(2)20(21(22)17-10-9-16(26)11-18(17)27)23(29)32-13-15-7-5-4-6-8-15/h4-11H,3,12-13H2,1-2H3
915296-81-0Relevant articles and documents
Optimization of activity, selectivity, and liability profiles in 5-oxopyrrolopyridine DPP4 inhibitors leading to clinical candidate (Sa)-2-(3-(aminomethyl)-4-(2,4-dichlorophenyl)-2-methyl-5-oxo-5H-pyrrolo[3,4-b] pyridin-6(7H)-yl)-N, N-dimethylacetamide (BMS-767778)
Devasthale, Pratik,Wang, Ying,Wang, Wei,Fevig, John,Feng, Jianxin,Wang, Aiying,Harrity, Tom,Egan, Don,Morgan, Nathan,Cap, Michael,Fura, Aberra,Klei, Herbert E.,Kish, Kevin,Weigelt, Carolyn,Sun, Lucy,Levesque, Paul,Moulin, Frederic,Li, Yi-Xin,Zahler, Robert,Kirby, Mark S.,Hamann, Lawrence G.
, p. 7343 - 7357 (2013/10/21)
Optimization of a 5-oxopyrrolopyridine series based upon structure-activity relationships (SARs) developed from our previous efforts on a number of related bicyclic series yielded compound 2s (BMS-767778) with an overall activity, selectivity, efficacy, PK, and developability profile suitable for progression into the clinic. SAR in the series and characterization of 2s are described.
Pyrrolopyridine-based inhibitors of dipeptidyl peptidase IV and methods
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Page/Page column 36, (2008/06/13)
Compounds are provided having the formula (I) wherein R, X, Y, Z, A and n are as defined herein, which are inhibitors of dipeptidyl peptidase IV and thus are useful in treating diabetes and related diseases.
