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5,6,7,8,9,10-Hexahydro-cyclohepta[b]quinolin-11-one is a complex organic compound with the molecular formula C14H19NO. It is a derivative of cyclohepta[b]quinoline, a tricyclic aromatic system, with six hydrogen atoms added to the ring structure, resulting in a hexahydro (six-hydrogen) addition. The compound features a ketone functional group at the 11-position, which is a carbonyl group (C=O) bonded to an alkyl group. This ketone group is a key structural feature that influences the compound's reactivity and properties. The hexahydro-cyclohepta[b]quinolin-11-one is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and functional groups.

5220-39-3

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5220-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5220-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5220-39:
(6*5)+(5*2)+(4*2)+(3*0)+(2*3)+(1*9)=63
63 % 10 = 3
So 5220-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO/c16-14-10-6-2-1-3-8-12(10)15-13-9-5-4-7-11(13)14/h4-5,7,9H,1-3,6,8H2,(H,15,16)

5220-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8,9,10-hexahydrocyclohepta[b]quinolin-11-one

1.2 Other means of identification

Product number -
Other names 5,6,7,8,9,10-Hexahydro-cyclohepta[b]quinolin-11-one

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:5220-39-3 SDS

5220-39-3Relevant academic research and scientific papers

A new class of histamine H3-receptor antagonists: Synthesis and structure - Activity relationships of 7,8,9,10-Tetrahydro-6H-cyclohepta[b]quinolines

Turner, Sean C.,Esbenshade, Timothy A.,Bennani, Youssef L.,Hancock, Arthur A.

, p. 2131 - 2135 (2007/10/03)

The synthesis and biological evaluation of novel cycloheptaquinoline antagonists of the human H3 receptor are described. Two series of compounds, bearing either an amino substituent or an alkyne linker at the 11-position, were investigated. Modifications of the amino substituents, optimization of chain length and the effect of conformational restraints are described. Several compounds with high affinity and selectivity for the H3 receptor were discovered.

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