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7140-32-1

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7140-32-1 Usage

Description

Cyclotridec[b]indole, dodecahydro-, also known as dihydrochanna, is a polycyclic aromatic hydrocarbon featuring three fused indole rings and twelve hydrogen atoms. This crystalline solid has a molecular weight of 390.651 g/mol and is not readily soluble in water, but it is soluble in organic solvents such as ethanol and acetone.

Uses

Used in Pharmaceutical Industry:
Cyclotridec[b]indole, dodecahydrois used as a chemical compound for research purposes in the pharmaceutical industry. Its unique structure and properties make it a potential candidate for the development of new drugs and therapeutic agents.
Used in Chemical Industry:
In the chemical industry, Cyclotridec[b]indole, dodecahydrois utilized for research and development of new chemical products. Its solubility in organic solvents allows for its use in various chemical reactions and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 7140-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7140-32:
(6*7)+(5*1)+(4*4)+(3*0)+(2*3)+(1*2)=71
71 % 10 = 1
So 7140-32-1 is a valid CAS Registry Number.

7140-32-1Downstream Products

7140-32-1Relevant articles and documents

2,3-Disubstituted indoles from olefins and hydrazines via tandem hydroformylation-Fischer indole synthesis and skeletal rearrangement

Linnepe, Petra,Schmidt, Axel M.,Eilbracht, Peter

, p. 302 - 313 (2007/10/03)

The tandem hydroformylation-Fischer indolisation protocol is used in the synthesis of 2,3-disubstituted indoles. After hydroformylation of selected olefins to form α-branched aldehydes in a one-pot procedure these are condensed with phenylhydrazine to give hydrazones. Upon acid-promoted [3,3]-sigmatropic rearrangement indolenine intermediates with quaternary centres in the 3-position are formed, which, after selective Wagner-Meerwein-type rearrangement of one of the substituents from the 3- to the 2-position, lead to 2,3-disubstituted indoles. Several olefins, bearing substituents with various functional groups, as well as cyclic olefinic systems are investigated. The Royal Society of Chemistry 2006.

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