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2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE is a pyrrole derivative chemical compound with the formula C13H13N3O. It features a furfuryl group attached to the amino moiety and a carbonitrile group at the 3-position of the pyrrole ring. 2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE has been investigated for its potential biological activities and is considered for use as a drug or pharmaceutical intermediate. Careful handling and adherence to safety protocols are essential when working with this chemical in a laboratory environment.

103026-02-4

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103026-02-4 Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE is used as a potential drug or pharmaceutical intermediate due to its studied biological activities. Its unique structure and properties make it a candidate for further research and development in the creation of new medications or as a component in existing ones.
Used in Research and Development:
In the field of scientific research, 2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE serves as a subject for exploration into its biological activities and potential applications. Researchers utilize 2-AMINO-1-(2-FURYLMETHYL)-4,5-DIMETHYL-1H-PYRROLE-3-CARBONITRILE to study its interactions with biological systems and to understand its mechanisms of action, which can contribute to the advancement of medical and pharmaceutical sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 103026-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,2 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103026-02:
(8*1)+(7*0)+(6*3)+(5*0)+(4*2)+(3*6)+(2*0)+(1*2)=54
54 % 10 = 4
So 103026-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O/c1-8-9(2)15(12(14)11(8)6-13)7-10-4-3-5-16-10/h3-5H,7,14H2,1-2H3

103026-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(furan-2-ylmethyl)-4,5-dimethylpyrrole-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-3-carbonitrile,2-amino-1-(2-furanylmethyl)-4,5-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:103026-02-4 SDS

103026-02-4Relevant articles and documents

Synthesis and rearrangements of 7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]-and 7h-pyrrolo[3,2-e][1,2,4]triazolo[4,3-c]pyrimidines

Vorob'ev,Kurbatov,Krasnikov,Mezheritskii,Usova

, p. 1492 - 1497 (2007/10/03)

7H-Pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidines were synthesized by the reactions of 2-ethoxymethyleneamino-1H-pyrrole-3-carbonitriles with acid hydrazides and by the reactions of aminoiminopyrimidines (prepared based on the above-mentioned carbonitriles) with acid chlorides.

Synthesis of 7-Unsubstituted 7H-Pyrrolopyrimidines

Pichler, Herbert,Folkers, Gerd,Roth, Hermann J.,Eger, Kurt

, p. 1485 - 1505 (2007/10/02)

The title compounds 4 are obtained by N-7 dealkylation of the 2-furanylmethyl, 2-thiophenylmethyl, or 1-phenylethyl group from 2a-g and 10 a-j with polyphosphoric acid.In contrast to the 2-furanylmethyl group the 2-thiophenylmethyl and 1-phenylethyl group

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