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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-chloro-N-(2-thiophen-2-ylimidazo[1,2-a]pyridin-3-yl)benzamide

Clc1ccc(cc1)C(=O)Nc1c(nc2n1cccc2)c1cccs1 Request for Quotation
Chemical Name: 4-chloro-N-(2-thiophen-2-ylimidazo[1,2-a]pyridin-3-yl)benzamide
CAS Number: 374084-31-8
Product Number: AG00CHNR(AGN-PC-0JYWA9)
Synonyms:
MDL No:
Molecular Formula: C18H12ClN3OS
Molecular Weight: 353.8254

Identification/Properties

Computed Properties
Molecular Weight:
353.824g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
353.039g/mol
Monoisotopic Mass:
353.039g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
458
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


DS2, also known as dicyclohexylcarbodiimide, is a versatile chemical reagent widely used in organic synthesis for coupling reactions. It acts as a zero displacement reagent, facilitating the formation of amide bonds between carboxylic acids and amines. DS2 serves as a coupling agent that activates carboxylic acids by converting them into reactive ester intermediates, which then react with amines to form amide linkages.In peptide synthesis, DS2 plays a crucial role in the formation of peptide bonds between amino acids, leading to the production of complex peptides and proteins. Its efficient activation of carboxylic acids allows for the selective and high-yield synthesis of peptides with desired sequences.Additionally, DS2 finds application in the preparation of esters, lactams, and other amide-containing compounds. Its compatibility with various functional groups and mild reaction conditions make it a preferred reagent in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Overall, DS2's role as a coupling agent in chemical synthesis enables the efficient and precise formation of amide bonds, making it an indispensable tool for organic chemists in the preparation of diverse compounds.