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2-IODO-2-PROPENAL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

99414-73-0

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99414-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99414-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99414-73:
(7*9)+(6*9)+(5*4)+(4*1)+(3*4)+(2*7)+(1*3)=170
170 % 10 = 0
So 99414-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H3IO/c1-3(4)2-5/h2H,1H2

99414-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodoprop-2-enal

1.2 Other means of identification

Product number -
Other names 2-Jod-acrylaldehyd

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:99414-73-0 SDS

99414-73-0Upstream product

99414-73-0Relevant academic research and scientific papers

Towards allopumiliotoxins: A concise synthesis of the indolizidine core

Vijaykumar, Bodduri V. D.,Mallesham, Pitchakuntla,Chandrasekhar, Srivari

experimental part, p. 988 - 994 (2012/04/04)

The common bicyclic indolizidine core present in several allopumiliotoxins was synthesized by the sequential use of a Crimmins' aldol reaction, an SOCl2-mediated SNi displacement, and an intramolecular nucleophilic acyl substitution (INAS) as the key transformations. A concise synthesis of the indolizidine core of allopumiliotoxins is described by using an aldol reaction, an SNi displacement and an intramolecular nucleophilic acyl substitution as key steps. Copyright

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