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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)-

Cyclohexaneacetic acid, a-amino-, hydrochloride, (aS)-

N[C@H](C(=O)O)C1CCCCC1.Cl Request for Quotation
Chemical Name: Cyclohexaneacetic acid, a-amino-, hydrochloride, (aS)-
CAS Number: 191611-20-8
Product Number: AG002FDJ(AGN-PC-0QKMBC)
Synonyms:
MDL No:
Molecular Formula: C8H16ClNO2
Molecular Weight: 193.6711

Identification/Properties

Computed Properties
Molecular Weight:
193.671g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
193.087g/mol
Monoisotopic Mass:
193.087g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
141
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-Amino-2-cyclohexylacetic acid hydrochloride, also known as $name$, serves as a valuable reagent in chemical synthesis processes. Its distinctive stereochemistry confers unique properties that make it a versatile building block in organic chemistry. This compound is particularly useful in asymmetric synthesis, where precise control over chiral centers is essential for producing enantiopure compounds. By incorporating (S)-2-Amino-2-cyclohexylacetic acid hydrochloride into synthetic routes, chemists can access a wide range of structurally diverse molecules with high stereochemical purity. Its application extends to the preparation of pharmaceutical intermediates, agrochemicals, and materials with tailored properties. Furthermore, the compatibility of this compound with various synthetic methodologies highlights its significance in contemporary organic chemistry research.