1. Home
  2. 8-Azabicyclo[3.2.1]octane-3-methanol, 8-methyl-

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)-

8-Azabicyclo[3.2.1]octane-3-methanol, 8-methyl-

OCC1CC2CCC(C1)N2C Request for Quotation
Chemical Name: 8-Azabicyclo[3.2.1]octane-3-methanol, 8-methyl-
CAS Number: 90949-82-9
Product Number: AG006GA9(AGN-PC-03JR5F)
Synonyms:
MDL No:
Molecular Formula: C9H17NO
Molecular Weight: 155.2374

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

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

Request for Quotation

Customer Feedback

Chemical Structure


(8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)methanol is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of complex organic molecules. Due to its unique structure and reactivity, this compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. It can undergo a range of functional group transformations, enabling the introduction of specific chemical moieties with high regio- and stereo-selectivity. Additionally, (8-Methyl-8-azabicyclo[3.2.1]octan-3-yl)methanol exhibits excellent compatibility with a variety of reaction conditions, making it an essential component in the development of novel synthetic methodologies and strategies. Its ability to participate in diverse chemical reactions highlights its importance in the establishment of efficient synthetic routes for the production of bioactive compounds and complex organic materials.