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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)-

Benzoic acid, 3,5-bis(aminomethyl)-, dihydrochloride

NCc1cc(CN)cc(c1)C(=O)O.Cl.Cl Request for Quotation
Chemical Name: Benzoic acid, 3,5-bis(aminomethyl)-, dihydrochloride
CAS Number: 185963-32-0
Product Number: AG00AO80(AGN-PC-0QEWSX)
Synonyms:
MDL No:
Molecular Formula: C9H14Cl2N2O2
Molecular Weight: 253.1257

Identification/Properties

Computed Properties
Molecular Weight:
253.123g/mol
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
252.043g/mol
Monoisotopic Mass:
252.043g/mol
Topological Polar Surface Area:
89.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
173
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:
3
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Bis(aminomethyl)benzoic acid dihydrochloride is a versatile compound commonly used in chemical synthesis processes. Its unique structure and properties make it an essential component in the creation of complex organic molecules and pharmaceutical intermediates. The compound serves as a valuable building block in the synthesis of various biologically active compounds due to its ability to undergo selective reactions and form specific chemical bonds. Additionally, 3,5-Bis(aminomethyl)benzoic acid dihydrochloride plays a crucial role in the development of new materials, such as polymers and coordination complexes, through controlled chemical reactions and functional group manipulations. Its application in chemical synthesis extends to the preparation of molecular probes, dyes, and ligands for catalysis, highlighting its significance in the field of organic chemistry.