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2-PHENYL-INDOLIZINE-3-CARBALDEHYDE is a heterocyclic chemical compound with the molecular formula C20H14N2O. It features an indolizine ring structure with a phenyl group and a carbaldehyde functional group attached, which endows it with unique structural and chemical properties.

3672-41-1

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3672-41-1 Usage

Uses

Used in Pharmaceutical Industry:
2-PHENYL-INDOLIZINE-3-CARBALDEHYDE is used as a key intermediate in the synthesis of various organic compounds for drug development. Its unique structure and chemical properties make it a promising candidate for the creation of new pharmaceuticals with potential biological activities.
Used in Agrochemical Industry:
In the agrochemical sector, 2-PHENYL-INDOLIZINE-3-CARBALDEHYDE is utilized as a building block for the development of novel agrochemicals. Its chemical properties allow it to be incorporated into the design of new compounds with potential applications in agriculture.
Used in Specialty Chemicals Production:
2-PHENYL-INDOLIZINE-3-CARBALDEHYDE is used as a raw material in the production of dyes, perfumes, and other specialty chemicals. Its distinctive structure contributes to the development of unique and high-quality products in these industries.
Further research and exploration of 2-PHENYL-INDOLIZINE-3-CARBALDEHYDE's properties are necessary to fully understand and maximize its potential uses across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3672-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3672-41:
(6*3)+(5*6)+(4*7)+(3*2)+(2*4)+(1*1)=91
91 % 10 = 1
So 3672-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO/c17-11-15-14(12-6-2-1-3-7-12)10-13-8-4-5-9-16(13)15/h1-11H

3672-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylindolizine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Phenyl-3-formyl-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:3672-41-1 SDS

3672-41-1Downstream Products

3672-41-1Relevant academic research and scientific papers

HETEROCYCLIC SYNTHESIS BY ELECTROCYCLIZATION OF EXTENDED DIPOLES: A NOVEL ACCESS TO THE INDOLIZINE AND QUINOLIZINE SYSTEMS

Eberbach, Wolfgang,Maier, Wolfram

, p. 5591 - 5594 (2007/10/02)

On thermal activation α-butenynyl substituted pyridine-N-oxides 4 undergo a multistep rearrangement affording 4-oxo-4H-quinolizines (8) and 2-acylindolizines (9).In the geometrical isomeriziation of E-4 to Z-4 annulated isoxazolidines (7) are involved as unstable intermediates.

Direct positive dyes made from 3-indolizine carboxaldehyde

-

, (2008/06/13)

A new group of cyanine and merocyanine spectral sensitizing dyes based on derivatives of 3-indolizine carboxaldehyde is particularly useful in sensitizing a direct positive silver halide emulsion to orange and red.

SYNTHESIS OF VINYL-SUBSTITUTED INDOLIZINE DERIVATIVES BY A NOVEL REACTION OF INDOLIZINES WITH ETHOXYETHYLENES HAVING ELECTRON WITHDRAWING SUBSTITUENTS

Yamashita, Yoshiro,Suzuki, Daisuke,Masumura, Mitsuo

, p. 1499 - 1502 (2007/10/02)

Reactions of indolizine derivatives with electron deficient ethoxyethylenes such as ethoxymethylenemalononitrile gave vinyl-substituted indolizines 3 by the Michael type addition reaction followed by ethanol elimination.Hydrolysis of 3-dicyanovinylindolizines afforded 3-formylindolizines.

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