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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)-

Cyclohexanecarboxylicacid, 4,4'-[iminobis(methylene)]bis-, [trans(trans)]- (9CI)

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Chemical Name: Cyclohexanecarboxylicacid, 4,4'-[iminobis(methylene)]bis-, [trans(trans)]- (9CI)
CAS Number: 93940-19-3
Product Number: AG00GW7T(AGN-PC-0W3J9F)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
297.39g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
297.194008g/mol
Monoisotopic Mass:
297.194008g/mol
Topological Polar Surface Area:
86.6Ų
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
321
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


The (trans,trans)-4,4'-(Azanediylbis(methylene))dicyclohexanecarboxylic acid is a versatile compound widely used in chemical synthesis. With its unique molecular structure, this acid serves as a crucial building block in the creation of complex organic molecules. Its application in chemical synthesis is particularly prominent in the formation of various pharmaceutical compounds, agrochemicals, and specialty materials. By incorporating this acid into reaction pathways, chemists can efficiently construct intricate molecular architectures, allowing for the development of new drugs, crop protection agents, and advanced materials. Furthermore, the acid's reactivity and stability make it a valuable tool in the synthesis of stereochemically pure compounds, essential for drug discovery and material science research.