6883-81-4

Basic information

• Product Name: 2-Naphthalenemethanol, 5,6,7,8-tetrahydro-
• Synonyms: 2-Naphthalenemethanol, 5,6,7,8-tetrahydro- ;(5,6,7,8-tetrahydronaphthalen-2-yl)methanol;2-NAPHTHALENECARBOXYLIC ACID, 5,6,7,8-TETRAHYDRO-
• CAS NO: 6883-81-4
• Molecular Formula: C₁₁H₁₄O
• Molecular Weight: 162.22826
• Mol File: 6883-81-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Naphthalenemethanol, 5,6,7,8-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenemethanol, 5,6,7,8-tetrahydro-(6883-81-4)
• EPA Substance Registry System: 2-Naphthalenemethanol, 5,6,7,8-tetrahydro-(6883-81-4)

Safety Data

• Hazardous Substances Data: 6883-81-4(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 119-64-2 tetralin 
• 64-17-5 ethanol 
• 51529-97-6 5,6,7,8-tetrahydronaphthalene-2-carbaldehyde 
• 7705-08-0 iron(III) chloride 

Downstream Products

• 91-57-6 2-Methylnaphthalene 
• 53618-53-4 (5,6,7,8-Tetrahydro-naphthalen-2-ylmethanesulfinyl)-acetic acid 4-nitro-benzyl ester 
• 53618-54-5 (5,6,7,8-Tetrahydro-naphthalen-2-ylmethanesulfinyl)-acetic acid 2-(4-bromo-phenyl)-2-oxo-ethyl ester 
• 1131-63-1 1,2,3,4-tetrahydro-2-naphthoic acid 
• 125868-80-6 2-(o-Carboxybenzyl)-(6,7,8,9-tetrahydrobenzoindan)-1-on 
• 6836-48-2 6-(bromomethyl)-1,2,3,4-tetrahydronaphthalene 
• 51629-67-5 2-(4-Chloro-phenyl)-3-methyl-butyric acid 5,6,7,8-tetrahydro-naphthalen-2-ylmethyl ester 
• 1680-51-9 6-methyl-1,2,3,4-tetrahydronaphthalene 
• 51529-97-6 5,6,7,8-tetrahydronaphthalene-2-carbaldehyde 
• 3160-18-7 <6-(1,2,3,4-tetrahydronaphthalenyl)>acetonitrile 

Relevant articles and documents

SYNTHESIS OF TRICYCLIC BENZAZEPINES AND THEIR DOPAMINE D1- AND D2-AFFINITY

A new group of angular 8,9-annelated 3-benzazepines has been found to be potent and selective dopamine D1-receptor antagonists of interest as possible pharmaceuticals in the treatment of schizophrenia.The synthesis of three new conformationally constrained representatives of this group of benzazepines is described and their affinity to the D1-receptor evaluated.Although none of these proved superior to the previously examined compounds, useful information on the receptor binding site was obtained.