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1H-Pyrrole,1-(3-chloro-4-fluorophenyl)-2,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1692-00-8

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1692-00-8 Usage

Chemical structure

A pyrrole ring with a chloro-fluoro substituted phenyl ring and two methyl groups attached

Usage

Building block for the synthesis of various drug molecules in the pharmaceutical industry

Biological activity

Exhibits potential biological activity and is being studied for its therapeutic properties

Additional use

Can be used as a reagent in organic synthesis for the preparation of other complex chemical compounds

Safety precautions

Should be handled and used with caution due to its potential hazards and toxicity.

Check Digit Verification of cas no

The CAS Registry Mumber 1692-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1692-00:
(6*1)+(5*6)+(4*9)+(3*2)+(2*0)+(1*0)=78
78 % 10 = 8
So 1692-00-8 is a valid CAS Registry Number.

1692-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Chlor-4-fluorphenyl)-2,5-dimethyl-pyrrol

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole,1-(3-chloro-4-fluorophenyl)-2,5-dimethyl-

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:1692-00-8 SDS

1692-00-8Downstream Products

1692-00-8Relevant academic research and scientific papers

Bio-based material as medium, mild and reusable catalyst for paal–knorr pyrrole synthesis with and without ultrasonic irradiation

Sharma, Abha,Kalyani, Illa Siva,Fatima, Anam

supporting information, p. 226 - 232 (2018/03/09)

Background: Pyrrole moiety is found in naturally occurring compounds such as chlorophyll, haem, and vitamin B12 and present in a number of drugs for example atorvastatin, ketorolac, elopiprazole, tolmetin and sunitinib. Various methods have been used for the synthesis of pyrrole derivatives; however, still there is a need for environmentally benign and economic protocol. Method: We have reported a simple, mild and speedy synthesis of N-substituted 2,5-dimethyl pyrrole derivatives in ‘’GAAS’’ as medium and catalyst at room temperature and under ultrasound irradiation. Results: This protocol was employed for the synthesis of various 2,5-dimethyl-N-substituted pyrrole-derivatives using both aliphatic as well as aromatic amines in short time (2 to 10 minutes)with excellent yield (84-95%) at room temperature and under ultrasonic irradiation. The catalytic system “GAAS’’ was regenerated and reused five times effectively without major loss of activity. Conclusion: In conclusion, we have developed an eco-friendly, simple, faster, reusable, mild, and efficient protocol for the synthesis of N-substituted pyrrole derivatives. This bio-based protocol is cost-effective and greener methodology for the synthesis of biologically active N-substituted pyrrole derivatives.

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