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6,7-dihydro-5H-dibenzo[c,g]carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63397-99-9

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63397-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63397-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,9 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63397-99:
(7*6)+(6*3)+(5*3)+(4*9)+(3*7)+(2*9)+(1*9)=159
159 % 10 = 9
So 63397-99-9 is a valid CAS Registry Number.

63397-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dihydro-5H-dibenzo[c,g]carbazole

1.2 Other means of identification

Product number -
Other names 5,6-Dihydro-7H-dibenzo[c,g]carbazol

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:63397-99-9 SDS

63397-99-9Downstream Products

63397-99-9Relevant academic research and scientific papers

Structure of dinaphtho[2,1-b:1,2'-d]-five-membered ring aromatic heterocycles

Fabbri, Davide,Dore, Antonio,Gladiali, Serafino,De Lucchi, Ottorino,Valle, Giovanni

, p. 11 - 18 (2007/10/03)

A comparison between the X-ray structures of a series of binaphthyl-substituted five-membered aromatic heterocycles la-e, comprising pyrrole, furan, phosphole, thiophene and others, enlightens the effect of the heteroatom on the distortion of the molecules and the differences with the fully aromatic helicene, If (dibenzophenanth'ene). The X-ray data were either taken from the literature (le, le and If) or from compounds prepared in the course of the present study (la and Id). The furan Ib has also been prepared by new methods but its crystals were not suitable for X-ray analysis. The X-ray structures of the tetrahydro-substituted nitrogen and oxygen heterocycles 2a and 2b are also reported. The energy barrier to racemization has been determ ned by line-shape analysis of VT-NMR spectra for those.molecules where the presence of a substituent at the heteroatom and a high pyramidal inversion barrier render the naphthyl protons at the 1 and 13 position non equivalent (i.e. in le, Id', and Id").

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