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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)-

5H-Cyclopenta[b]pyridin-7-ol,6,7-dihydro-, (7S)-

O[C@H]1CCc2c1nccc2 Request for Quotation
Chemical Name: 5H-Cyclopenta[b]pyridin-7-ol,6,7-dihydro-, (7S)-
CAS Number: 887921-99-5
Product Number: AG008B3N(AGN-PC-0VNYC5)
Synonyms:
MDL No:
Molecular Formula: C8H9NO
Molecular Weight: 135.1632

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-6,7-Dihydro-5H-cyclopenta[b]pyridin-7-ol, commonly known as $name$, is a versatile compound widely used in chemical synthesis. One of its key applications lies in its ability to act as a chiral building block in organic reactions. Due to its unique structure, $name$ can serve as a valuable starting material for the synthesis of various complex molecules with specific stereochemical configurations. Its presence can impart chirality to the final products, making it a valuable tool in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, (S)-6,7-Dihydro-5H-cyclopenta[b]pyridin-7-ol plays a crucial role in asymmetric synthesis, enabling the production of enantiopure compounds with high levels of stereocontrol. Its utility in chemical transformations makes it a sought-after reagent in the field of organic chemistry, facilitating the creation of diverse molecular structures with precise stereochemistry.