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Pyrrolo[2,1-a]isoquinoline is a heterocyclic organic compound with the molecular formula C13H10N2. It is a tricyclic structure consisting of a pyrrole ring fused to an isoquinoline ring, which is a benzene ring with two nitrogen atoms at adjacent positions. Pyrrolo[2,1-a]isoquinoline is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various bioactive molecules. Due to its unique structure, pyrrolo[2,1-a]isoquinoline can form part of complex molecular frameworks that exhibit a range of pharmacological properties, making it a subject of interest in drug discovery and development.

234-92-4

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234-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 234-92-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 234-92:
(5*2)+(4*3)+(3*4)+(2*9)+(1*2)=54
54 % 10 = 4
So 234-92-4 is a valid CAS Registry Number.

234-92-4SDS

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 pyrrolo[2,1-a]isoquinoline

1.2 Other means of identification

Product number -
Other names Benz<g>indolizin

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:234-92-4 SDS

234-92-4Downstream Products

234-92-4Relevant academic research and scientific papers

Synthesis of Cyclazine and Benzocyclazine Derivatives by Use of the Cycloaddition Reaction of Indolizines and Dimethyl Acetylenedicarboxylate

Tominaga, Yoshinori,Shiroshita, Yoshihide,Kurokawa, Tomohiko,Gotou, Hiromi,Matsuda, Yoshiro,Hosomi, Akira

, p. 477 - 487 (2007/10/02)

The reaction of 1-ethoxycarbonylmethylpyridinium bromides 5a-k with nitro ketene dithioacetal, 1,1-bis(methylthio)-2-nitroethylene (2), in the presence of triethylamine in ethanol gave the desired ethyl 2-methylthioindolizine-3-carboxylates 3a-k in good y

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