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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)-

Benzenemethanol, 3-hydroxy-a-[(methylamino)methyl]-, hydrochloride,(S)-

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Chemical Name: Benzenemethanol, 3-hydroxy-a-[(methylamino)methyl]-, hydrochloride,(S)-
CAS Number: 939-38-8
Product Number: AG00GWLD(AGN-PC-0W3JB6)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
203.666g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
203.071g/mol
Monoisotopic Mass:
203.071g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
130
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


(S)-Phenylephrine Hydrochloride, a synthetic catecholamine and sympathomimetic agent, plays a crucial role in chemical synthesis as a chiral building block. Its chiral nature, defined by the (S)-stereoisomer, makes it a valuable tool in the production of enantiomerically pure compounds. In asymmetric synthesis, (S)-Phenylephrine Hydrochloride serves as a key reagent for creating molecules with specific chirality, thereby enabling the development of pharmaceuticals, agrochemicals, and other fine chemicals. By incorporating (S)-Phenylephrine Hydrochloride into various reactions, chemists can access stereochemically intricate structures essential for both basic research and industrial applications.