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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)-

Benzeneacetic acid, a-cyclohexyl-a-hydroxy-, (aS)-

OC(=O)[C@@](c1ccccc1)(C1CCCCC1)O Request for Quotation
Chemical Name: Benzeneacetic acid, a-cyclohexyl-a-hydroxy-, (aS)-
CAS Number: 20585-34-6
Product Number: AG00BDF8(AGN-PC-0QVMFC)
Synonyms:
MDL No:
Molecular Formula: C14H18O3
Molecular Weight: 234.2909

Identification/Properties

Properties
MP:
143-145°C
BP:
408.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-Cyclohexyl-2-hydroxy-2-phenylacetic acid, also known as a key chiral building block in organic chemistry, plays a crucial role in chemical synthesis. This compound exhibits enantioselectivity, making it highly valuable in the production of pharmaceuticals, agrochemicals, and specialty materials. Its cyclohexyl and phenyl substituents provide structural diversity and versatility, allowing for various functional group manipulations in synthetic pathways.In chemical synthesis, (S)-2-Cyclohexyl-2-hydroxy-2-phenylacetic acid serves as a chiral auxiliary or ligand, enabling asymmetric transformations and controlling the stereochemistry of the final products. Its presence can lead to the formation of specific enantiomers, crucial in drug discovery and development. Additionally, this compound is utilized in the preparation of complex molecules such as natural products, where precise stereochemical control is essential for their biological activity.By incorporating (S)-2-Cyclohexyl-2-hydroxy-2-phenylacetic acid into synthetic routes, chemists can access enantiomerically pure compounds with high levels of stereocontrol, opening up possibilities for the creation of new materials and active pharmaceutical ingredients. This compound's unique chirality and reactivity make it a valuable tool in the synthesis of diverse chemical entities, highlighting its significance in modern organic chemistry practices.