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887922-92-1

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887922-92-1 Usage

General Description

4-ISOCYANATO-1-METHYL-1H-INDOLE is a chemical compound with the formula C10H8N2O. It is an isocyanate derivative with a methyl and indole group, and is commonly used in the synthesis of pharmaceuticals, agrochemicals, and dyes. Isocyanates are highly reactive and are known to cause skin and respiratory sensitization, irritation, and even allergic reactions if not handled properly. Therefore, strict safety precautions and proper handling are necessary when working with this chemical. It is important to use appropriate protective equipment and work in a well-ventilated area when dealing with 4-ISOCYANATO-1-METHYL-1H-INDOLE to avoid any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 887922-92-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,9,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 887922-92:
(8*8)+(7*8)+(6*7)+(5*9)+(4*2)+(3*2)+(2*9)+(1*2)=241
241 % 10 = 1
So 887922-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O/c1-12-6-5-8-9(11-7-13)3-2-4-10(8)12/h2-6H,1H3

887922-92-1SDS

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 4-isocyanato-1-methylindole

1.2 Other means of identification

Product number -
Other names 4-isocyanato-1-methyl-1H-indole

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:887922-92-1 SDS

887922-92-1Downstream Products

887922-92-1Relevant 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 (2006)

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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