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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)-

(S)-1-(5-Bromopyridin-2-yl)pyrrolidin-3-ol

O[C@H]1CCN(C1)c1ccc(cn1)Br Request for Quotation
Chemical Name: (S)-1-(5-Bromopyridin-2-yl)pyrrolidin-3-ol
CAS Number: 946002-90-0
Product Number: AG00H5S7(AGN-PC-0WAHY8)
Synonyms:
MDL No:
Molecular Formula: C9H11BrN2O
Molecular Weight: 243.1004

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
243.104g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
242.005g/mol
Monoisotopic Mass:
242.005g/mol
Topological Polar Surface Area:
36.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-1-(5-Bromopyridin-2-yl)pyrrolidin-3-ol compound is a versatile building block in chemical synthesis. Its unique structure makes it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Due to its chiral nature, this compound can be utilized in asymmetric synthesis to access enantiomerically pure molecules. Additionally, the bromopyridine moiety in the structure enables it to participate in transition metal-catalyzed cross-coupling reactions, facilitating the creation of complex molecular structures.Overall, the (S)-1-(5-Bromopyridin-2-yl)pyrrolidin-3-ol compound plays a crucial role in the synthesis of diverse chemical compounds with applications in multiple industries.