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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)-

N-Boc-(1S, 2R)-diaminocyclohexane (R)-Hydroxyphenylaceticacid salt

O[C@H](c1ccccc1)C(=O)O.O=C(OC(C)(C)C)N[C@H]1CCCC[C@H]1N Request for Quotation
Chemical Name: N-Boc-(1S, 2R)-diaminocyclohexane (R)-Hydroxyphenylaceticacid salt
CAS Number: 1391731-16-0
Product Number: AG003VGN(AGN-PC-0WAM0V)
Synonyms:
MDL No:
Molecular Formula: C19H30N2O5
Molecular Weight: 366.4519

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Computed Properties
Molecular Weight:
366.458g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
366.215g/mol
Monoisotopic Mass:
366.215g/mol
Topological Polar Surface Area:
122A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
361
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl ((1S,2R)-2-aminocyclohexyl)carbamate (R)-2-hydroxy-2-phenylacetate is a versatile compound commonly employed in chemical synthesis as a chiral building block. Its unique structure and reactivity make it a valuable reagent for the preparation of complex molecules with defined stereochemistry. In particular, this compound is utilized in the synthesis of pharmaceuticals, agrochemicals, and various biologically active compounds where precise control over the chiral configuration is crucial. By incorporating tert-Butyl ((1S,2R)-2-aminocyclohexyl)carbamate (R)-2-hydroxy-2-phenylacetate into synthetic routes, chemists can access enantiopure intermediates and final products, enabling the production of high-quality and potent compounds. This compound's application in chemical synthesis underscores its significance as a key component in the construction of advanced molecular structures with specific stereochemical properties.