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1,3,4,5-Tetrahydrobenzo[cd]indole-5-one is a chemical compound with the molecular formula C11H11NO. It is a derivative of benzo[c]indole, a tricyclic aromatic compound with a central indole nucleus. This specific compound is characterized by the presence of a carbonyl group at the 5-position and four hydrogen atoms attached to the carbon atoms at positions 1, 3, 4, and 5, which contribute to its tetrahydro structure. It is an organic molecule that can be found in various natural products and may have potential applications in the synthesis of pharmaceuticals and other organic compounds. Due to its complex structure, it is typically synthesized through multi-step chemical reactions and is of interest to researchers in the field of organic chemistry.

3744-82-9

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3744-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3744-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3744-82:
(6*3)+(5*7)+(4*4)+(3*4)+(2*8)+(1*2)=99
99 % 10 = 9
So 3744-82-9 is a valid CAS Registry Number.

3744-82-9SDS

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-Oxo-1,3,4,5-tetrahydrobenz[cd]indole

1.2 Other means of identification

Product number -
Other names 3,4-Dihydrobenz[cd]indol-5(1H)-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:3744-82-9 SDS

3744-82-9Relevant academic research and scientific papers

Dehydrogenation with Benzeneseleninic Anhydride in the Total Synthesis of Ergot Alkaloids

Ninomiya, Ichiya,Hashimoto, Chiyomi,Kiguchi, Toshiko,Naito, Takeaki,Barton, Derek, H. R.,et al.

, p. 707 - 713 (2007/10/02)

Investigation of the dehydrogenative conversion of indolines into indoles with benzeneseleninic anhydride (1) resulted in the development of an efficient standardised procedure, which was successfully applied to the final steps in first total synthesis of (+/-)-lysergol (18), (+/-)-isolysergol (27), and (+/-)-elymoclavine (29).

AN IMPROVED PROCEDURE FOR THE CONVERSION OF INDOLINES INTO INDOLES

Ninomiya, Ichiya,Kiguchi, Toshiko,Hashimoto, Chiyomi,Barton, Derek H. R.,Lusinchi, Xavier,Milliet, Pierre

, p. 4183 - 4186 (2007/10/02)

The addition of a sacrificial enamine (such as indole), or of a vinyl ether (like dihydropyran) to an indoline during dehydrogenation by phenylseleninic anhydride dramatically improves the yield of the corresponding indole.This is due to scavenging of Se

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