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884507-16-8

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884507-16-8 Usage

General Description

5-Isocyanato-1-methyl-1H-indole, also known as 1-methyl-5-isocyanatoindole, is a chemical compound with the molecular formula C10H8N2O. It is a derivative of indole and isocyanate, and has a pale yellow color. 5-Isocyanato-1-methyl-1H-indole is commonly used in the pharmaceutical industry as a building block for the synthesis of various biologically active compounds, including drugs and agrochemicals. It has also been studied for its potential use in the development of novel materials with applications in optoelectronics and organic electronics. 5-Isocyanato-1-methyl-1H-indole has been found to exhibit interesting properties and has attracted attention for its potential use in various industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 884507-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,5,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 884507-16:
(8*8)+(7*8)+(6*4)+(5*5)+(4*0)+(3*7)+(2*1)+(1*6)=198
198 % 10 = 8
So 884507-16-8 is a valid CAS Registry Number.

884507-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-isocyanato-1-methylindole

1.2 Other means of identification

Product number -
Other names 1H-Indole,5-isocyanato-1-methyl

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:884507-16-8 SDS

884507-16-8Downstream Products

884507-16-8Relevant articles and documents

Synthesis of highly substituted indole alkaloid species via [4+1] cyclization of nucleophilic carbenes and indole isocyanates

Rigby, James H.,Burke, Patrick J.

, p. 643 - 653 (2007/10/03)

Thermally induced [4+1] cyclization between indole isocyanates and dimethoxycarbene or bis(propylthio)carbene has been achieved with good chemical efficiency. The methodology provides rapid access to fused pyrroloindole substructures commonly found in a variety of indole alkaloid natural products.

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