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1130-93-4

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1130-93-4 Usage

General Description

CYCLOPENT[B]INDOLE, 1,2,3,4-TETRAHYDRO-7-METHYL- is a chemical compound that belongs to the class of indole compounds. It is a 1,2,3,4-tetrahydro derivative with a methyl group attached at the 7th position. CYCLOPENT[B]INDOLE, 1,2,3,4-TETRAHYDRO-7-METHYL- is a bicyclic structure containing a five-membered ring fused to an indole ring. It is used in research and pharmaceutical applications, where it may be used as a building block or intermediate in the synthesis of various organic compounds. The structure of CYCLOPENT[B]INDOLE, 1,2,3,4-TETRAHYDRO-7-METHYL- provides it with unique properties that make it valuable for use in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1130-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1130-93:
(6*1)+(5*1)+(4*3)+(3*0)+(2*9)+(1*3)=44
44 % 10 = 4
So 1130-93-4 is a valid CAS Registry Number.

1130-93-4SDS

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 7-methyl-1,2,3,4-tetrahydrocyclopenta[b]indole

1.2 Other means of identification

Product number -
Other names 7-Methyl-1,2,3,4-tetrahydro-cyclopenta<b>indol

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:1130-93-4 SDS

1130-93-4Downstream Products

1130-93-4Relevant articles and documents

Pd-Catalyzed Dearomatization of Indole Derivatives via Intermolecular Heck Reactions?

Yang, Ping,Xu, Ren-Qi,Zheng, Chao,You, Shu-Li

, p. 235 - 241 (2020)

Pd-catalyzed intermolecular dearomative Heck reaction of indoles with aryl iodides is described. The challenges on both reactivity and regioselectivity are addressed by the judicious regulation of the geometric and electronic properties of the substrates. An array of indoline derivatives bearing C2-quaternary center is obtained in good to excellent yields (up to 93%) with exclusive regioselectivity under operationally simple conditions. The mechanistic proposal is supported by detailed DFT calculations.

Fischer indole synthesis in the absence of a solvent

Matsumoto, Kiyoshi,Tanaka, Akinori,Yukio, Ikemi,Hayashi, Naoto,Toda, Mitsuo,Bulman, Robert A.

, p. 9 - 12 (2007/10/03)

The traditional Fischer synthesis of indoles has been investigated and it has been shown that the reaction proceeds in good yield in the absence of a solvent.

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