3015-19-8

Basic information

• Product Name: (1s,3s,5R,7S)-2-azaadaMantan-1-ol
• Synonyms: (1s,3s,5R,7S)-2-azaadaMantan-1-ol
• CAS NO: 3015-19-8
• Molecular Formula: C9H15NO
• Molecular Weight: 153.2215
• Mol File: 3015-19-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: (1s,3s,5R,7S)-2-azaadaMantan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (1s,3s,5R,7S)-2-azaadaMantan-1-ol(3015-19-8)
• EPA Substance Registry System: (1s,3s,5R,7S)-2-azaadaMantan-1-ol(3015-19-8)

Safety Data

• Hazardous Substances Data: 3015-19-8(Hazardous Substances Data)

Usage

General Description

(1s,3s,5R,7S)-2-azaadaMantan-1-ol is a chemical compound with a complex molecular structure. It is a stereochemically defined organic compound with four stereocenters, which means that it has four different arrangements of atoms around a stereogenic center, resulting in a chiral molecule. The compound is classified as an azaadamantane derivative, which is a bicyclic organic compound with nitrogen atoms in the ring structure. The "1-ol" suffix indicates that it contains a hydroxyl group, which makes it an alcohol. (1s,3s,5R,7S)-2-azaadaMantan-1-ol may have potential applications in pharmaceutical or chemical industries due to its unique structure and properties. Overall, (1s,3s,5R,7S)-2-azaadaMantan-1-ol is a complex and potentially versatile chemical compound with interesting stereochemical and functional group properties.

Upstream product

• 85616-64-4 3-Azidonoradamantane 
• 127666-15-3 tricyclo[3.3.1.0^3,7]nonyl-3-isocyanate 
• 85616-63-3 N-Noradamant-3-ylacetamide 
• 67064-09-9 3-noradamantanecarboxylic acid chloride 
• 28224-43-3 tricyclo[3.3.1.0^3,7]nonan-3-amine 
• 16200-53-6 3-noradamantanecarboxylic acid 
• 66077-97-2 spiro[bicyclo[3.3.1]nonane-3,2'-[1,3]dioxolan]-7-one 
• 905832-09-9 N-benzyloxycarbonyl-2-azaadamantane-1-ol 
• 770-15-0 bicyclo<3.3.1>nonane-3,7-dione 
• 85616-67-7 1-Methoxy-2-azaadamantane 
• 770-15-0 bicyclo[3.3.1]nonane-3,7-dione 
• 17933-29-8 7-methylenebicyclo[3.3.1]nonan-3-one 
• 5001-18-3 1,3-adamantandiol 
• 157521-81-8 7,7-ethylenedioxybicyclo[3.3.1]nonan-3-one oxime 

Downstream Products

• 57625-08-8 2-azatricyclo[3.3.1.1^3,7]dec-2-yloxidanyl 
• 768-41-2 2-azatricyclo[3.3.1.13,7 ]decane 

Relevant articles and documents

COMPOUNDS CONTAINING AN ALICYCLIE STRUCTURE AND ANTI-TUMOR APPLICATION

This invention relates with anti-tumor activities of new compounds containing an adamantyl group or analogs thereof. The invention also relates with the medication applications of anti-tumor and other diseases by this kind of compounds with the combination of S, P, T structures containing adamantyl group and the formation of stereoisomer, tautomers, prodrug, pharmaceutically acceptable salts, complex salts or solvates to their anticancer application and anticancer agents, which have the following general formula:

Photolytic Generation of Anti-Bredt Imines from 1-Azidobicyclooctane, 1-Azidobicyclononane, and 3-Azidonoradamantane

Photolysis of 1-azidobicyclooctane (18), 1-acidobicyclononane (24), and 3-azidonoradamantane (37) generated the corresponding bridgehead imines 12a, 13, 14, 15, and 16, respectively.These bridgehead imines were trapped spontaneously with sol