3,5-Pyridinedicarboxylic acid,1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-,2-[4-(diphenylmethyl)-1-piperazinyl]ethyl methyl ester, (4R)-


Chemical Name: 3,5-Pyridinedicarboxylic acid,1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-,2-[4-(diphenylmethyl)-1-piperazinyl]ethyl methyl ester, (4R)-
CAS Number: 133082-19-6
Product Number: AG00147U(AGN-PC-0PJXA5)
Synonyms:
MDL No:
Molecular Formula: C35H38N4O6
Molecular Weight: 610.6994

Identification/Properties


Computed Properties
Molecular Weight:
610.711g/mol
XLogP3:
5.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
11
Exact Mass:
610.279g/mol
Monoisotopic Mass:
610.279g/mol
Topological Polar Surface Area:
117A^2
Heavy Atom Count:
45
Formal Charge:
0
Complexity:
1090
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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Chemical Structure



This compound, 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 2-[4-(diphenylmethyl)-1-piperazinyl]ethyl methyl ester, (4R)-, is commonly utilized in chemical synthesis for its versatile properties and reactivity. In organic chemistry, it serves as a valuable intermediate in the development of various pharmaceuticals and agrochemicals. Its unique structural features make it a key building block in the creation of complex molecules through multi-step synthesis processes. The compound's chirality, represented by the (4R)-configuration, can play a crucial role in determining the stereochemistry of the final product, making it particularly useful in the synthesis of chiral compounds with specific biological activities. Overall, this compound's strategic incorporation into synthetic routes highlights its significance in enabling the creation of diverse chemical entities with desired properties.