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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)-

2-Pyrrolidinemethanol, hydrochloride, (S)-

OC[C@@H]1CCCN1.Cl Request for Quotation
Chemical Name: 2-Pyrrolidinemethanol, hydrochloride, (S)-
CAS Number: 79802-20-3
Product Number: AG00GHFW(AGN-PC-0OIAL8)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO
Molecular Weight: 137.60788

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Chemical Structure


(S)-Pyrrolidin-2-ylmethanol hydrochloride is a versatile compound commonly used in organic synthesis as a chiral building block. Its unique structure consisting of a pyrrolidine ring and a hydroxyl group makes it a valuable chemical intermediate in the preparation of various pharmaceuticals and fine chemicals. This compound is particularly useful in the asymmetric synthesis of biologically active molecules, where the chirality of the starting material plays a crucial role in determining the stereochemistry of the final product. Additionally, (S)-Pyrrolidin-2-ylmethanol hydrochloride can act as a catalyst or ligand in certain reactions, facilitating the formation of specific stereoisomers with high enantioselectivity. Its application in chemical synthesis extends to the production of specialty chemicals, agrochemicals, and materials with tailored properties.