1. Home
  2. benzyl (1S,5R)-3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

benzyl (1S,5R)-3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate

OC1CC2CCC(C1)N2C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: benzyl (1S,5R)-3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate
CAS Number: 92652-76-1
Product Number: AG00GSO5(AGN-PC-059B3M)
Synonyms:
MDL No:
Molecular Formula: C15H19NO3
Molecular Weight: 261.31626

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
261.321g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
261.136g/mol
Monoisotopic Mass:
261.136g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
313
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


Benzyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate is a versatile compound widely used in chemical synthesis as a key building block for the creation of complex organic molecules. Its unique structure allows it to participate in a variety of important chemical reactions, making it an essential intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.One of the main applications of Benzyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate is in the synthesis of heterocyclic compounds, where its cyclic structure and functional groups play a crucial role in forming intricate ring systems. Additionally, this compound can be utilized in the preparation of chiral molecules due to the presence of a stereocenter, enabling the development of enantiomerically pure products for use in the pharmaceutical industry.Furthermore, Benzyl 3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate serves as a valuable precursor for the production of bioactive compounds and natural products through various synthetic routes. Its incorporation into chemical reactions allows for the rapid and efficient construction of complex molecular frameworks, facilitating the discovery and development of novel compounds with potential therapeutic or industrial applications.