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100717-35-9

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100717-35-9 Usage

Type of compound

Aromatic organic compound

Class

Pyrroles (five-membered heterocyclic compounds)

Key structural feature

Contains a nitrogen atom

Usage

Chemical and pharmaceutical research

Application

Building block for the synthesis of various organic compounds

Potential applications

Development of new pharmaceutical drugs, production of organic materials, and fine chemicals

Reason for potential applications

Unique structural and chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 100717-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,1 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100717-35:
(8*1)+(7*0)+(6*0)+(5*7)+(4*1)+(3*7)+(2*3)+(1*5)=79
79 % 10 = 9
So 100717-35-9 is a valid CAS Registry Number.

100717-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-ethylphenyl)-2,5-dimethyl-1H-pyrrole

1.2 Other means of identification

Product number -
Other names 1-(2-Aethyl-phenyl)-2,5-dimethyl-pyrrol

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:100717-35-9 SDS

100717-35-9Downstream Products

100717-35-9Relevant articles and documents

-

Buu-Hoi

, p. 197,201 (1954)

-

Organometallic approach to the functionalization of alkyl groups containing 1-phenylpyrroles

Faigl, Ferenc,Vas Feldhoffer, Bernadett,Thurner, Angelika

, p. 2841 - 2849 (2007/10/03)

Novel regioselective methods have been developed for the mono- and difunctionalization of alkyl groups containing 1-phenylpyrroles using different organometallic reagents. Tailoring the reagents and conditions allowed us to prepare several new mono- and r

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