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250-91-9

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250-91-9 Usage

Chemical compound

4H-Furo[3,2-b]pyrrole

Class

Furo[3,2-b]pyrroles

Properties

Heterocyclic compound containing a furo-pyrrole ring system

Occurrence

Not naturally occurring

Main uses

Organic synthesis and medicinal chemistry research

Pharmacological activities

Investigated for anticancer, anti-inflammatory, and antiviral properties

Other studies

Potential as fluorescent dyes and materials in organic electronics

Importance

Molecule of interest for various research and application areas

Check Digit Verification of cas no

The CAS Registry Mumber 250-91-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 250-91:
(5*2)+(4*5)+(3*0)+(2*9)+(1*1)=49
49 % 10 = 9
So 250-91-9 is a valid CAS Registry Number.

250-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4H-furo[3,2-b]pyrrole

1.2 Other means of identification

Product number -
Other names furo<3,2-b>CTK1A0808

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:250-91-9 SDS

250-91-9Downstream Products

250-91-9Relevant articles and documents

ADDITION AND CYCLOADDITION REACTIONS OF FUROPYRROLES AND THEIR BENZO ANALOGUES: AN NMR STUDY OF STRUCTURE OF PRODUCTS

Krutosikova, Alzbeta,Dandarova, Miloslava,Alfoeldi, Juraj,Kovac,Jaroslav

, p. 1770 - 1778 (2007/10/02)

Reaction of furopyrroles and their benzo analogues with dimethyl butynedioate and ethyl propynoate were investigated.The reaction course is influenced by substituents on the system.Products of cycloaddition to the furan or pyrrole nucleus as well as products of Michael addition to the benzofuropyrrole system have been found.The structure of the products has been proven by 1H NMR and 13C NMR spectroscopy.

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