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3672-41-1

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3672-41-1 Usage

General Description

2-PHENYL-INDOLIZINE-3-CARBALDEHYDE is a chemical compound with the molecular formula C20H14N2O. It is a heterocyclic compound containing an indolizine ring structure with a phenyl group and a carbaldehyde functional group attached. 2-PHENYL-INDOLIZINE-3-CARBALDEHYDE has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and interesting chemical properties. It can be used in the synthesis of various organic compounds and may have biological activities that make it useful for drug development. Additionally, 2-PHENYL-INDOLIZINE-3-CARBALDEHYDE may also have industrial applications in the production of dyes, perfumes, and other specialty chemicals. Further research and exploration of its properties are needed to fully understand its potential uses.

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 articles and documents

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.

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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