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78739-83-0

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78739-83-0 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 52, p. 1922, 1987 DOI: 10.1021/jo00386a007

Check Digit Verification of cas no

The CAS Registry Mumber 78739-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78739-83:
(7*7)+(6*8)+(5*7)+(4*3)+(3*9)+(2*8)+(1*3)=190
190 % 10 = 0
So 78739-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H9IO/c10-5-7-6-11-9-4-2-1-3-8(7)9/h1-4,7H,5-6H2

78739-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(iodomethyl)-2,3-dihydro-1-benzofuran

1.2 Other means of identification

Product number -
Other names 2,3-dihydro-3-(iodomethyl)benzo{b}furan

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:78739-83-0 SDS

78739-83-0Upstream product

78739-83-0Relevant articles and documents

Free Radical Reactions in Synthesis. Homolysis of Alkylcobalt Complexes in the Presence of Radical-Trapping Agents

Patel, Vinod F.,Pattenden, Gerald

, p. 2703 - 2708 (2007/10/02)

Irradiations of the alkylcobalt salophen complexes (14), (21), (22), and (23) in the presence of radical-trapping agents, e.g. molecular oxygen, tetramethylpiperidine oxide, nitrogen monoxide, diphenyl disulphide, diphenyl diselenide, methanesulphonyl chloride, bromotrichloromethane, or iodine, leads to oxygen- , nitrogen- , sulphur/selenium- or halogen- (34) functionalised products.When these radical-trapping methodologies are combined with cobalt-mediated radical cyclisation reactions (Scheme 2) a powerful synthetic procedure, i.e. radical carbon-to-carbon bond formation with simultaneous functionalisation of the product radical centre, becomes available.

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