1. Home
  2. L-Proline, 4-cyclohexyl-, (4S)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

L-Proline, 4-cyclohexyl-, (4S)-

OC(=O)[C@H]1NC[C@@H](C1)C1CCCCC1 Request for Quotation
Chemical Name: L-Proline, 4-cyclohexyl-, (4S)-
CAS Number: 103201-78-1
Product Number: AG00389R(AGN-PC-0NVJTW)
Synonyms:
MDL No:
Molecular Formula: C11H19NO2
Molecular Weight: 197.2741

Identification/Properties

Computed Properties
Molecular Weight:
197.278g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
197.142g/mol
Monoisotopic Mass:
197.142g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

Request for Quotation

Customer Feedback

Chemical Structure


Trans-4-Cyclohexyl-L-Proline, also known as CHP, is a versatile compound widely used in chemical synthesis due to its unique chemical structure and properties. In organic chemistry, CHP serves as a valuable chiral building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its cyclic structure containing a proline moiety makes it an excellent precursor for the preparation of peptides and peptidomimetics with high stereochemical control. Additionally, CHP is commonly employed as a catalyst in asymmetric synthesis reactions to induce chirality in target molecules. Its cyclohexyl group provides steric hindrance, offering selectivity in reactions where stereochemistry is crucial. Overall, Trans-4-Cyclohexyl-L-Proline is an indispensable tool in the toolkit of synthetic chemists for achieving precise control over molecular structure and stereochemistry.