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5,6,7,8-Tetrahydrodibenzo[c,E]azocine is a complex organic compound with the molecular formula C16H17N. It is a derivative of dibenzoazocine, which is a tricyclic structure consisting of two benzene rings fused to a seven-membered azocine ring. 5,6,7,8-Tetrahydrodibenzo[c,E]azocine is characterized by its unique molecular structure, which features a partially saturated ring system, with four hydrogen atoms added to the parent dibenzoazocine structure. The presence of the nitrogen atom in the azocine ring imparts basic properties to the molecule, making it a potential candidate for various chemical and pharmaceutical applications. Due to its complex structure, 5,6,7,8-tetrahydrodibenzo[c,E]azocine may exhibit interesting chemical reactivity and could be further modified to explore its potential in drug development or other industrial applications.

6196-54-9

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6196-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6196-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6196-54:
(6*6)+(5*1)+(4*9)+(3*6)+(2*5)+(1*4)=109
109 % 10 = 9
So 6196-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H15N/c1-3-7-14-12(5-1)9-10-16-11-13-6-2-4-8-15(13)14/h1-8,16H,9-11H2

6196-54-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8-Tetrahydrodibenz[c,e]azocine

1.2 Other means of identification

Product number -
Other names 5,6,7,8-TETRAHYDRODIBENZ(C,E)AZOCINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6196-54-9 SDS

6196-54-9Upstream product

6196-54-9Downstream Products

6196-54-9Relevant academic research and scientific papers

A Convenient Synthesis of Apogalanthamine Analogues as α-Adrenergic Blocking Agents using Zerovalent Nickel

Kihara, Masaru,Itoh, Joji,Iguchi, Seiichiro,Imakura, Yasuhiro,Kobayashi, Shigeru

, p. 157 - 177 (2007/10/02)

The apogalanthamine analogues, 5,6,7,8-tetrahydrodibenzazocine (2) and its N-methyl and N-acetyl derivatives (1 and 3), and the methoxy derivatives (4, 5 and 9) of (1) were obtained in good yields by cyclization of the corresponding halogeno-N-benzyl-β-phenethylamines (10a, 11a-d, 12a,b and 13a-c) using stoichiometric amounts of zerovalent nickel generated in situ and potassium iodide.

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