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107616-56-8

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107616-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107616-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,1 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107616-56:
(8*1)+(7*0)+(6*7)+(5*6)+(4*1)+(3*6)+(2*5)+(1*6)=118
118 % 10 = 8
So 107616-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H11IO/c11-7-8-5-6-12-10-4-2-1-3-9(8)10/h1-4,8H,5-7H2

107616-56-8SDS

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 4-(iodomethyl)-3,4-dihydro-2H-chromene

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran,3,4-dihydro-4-(iodomethyl)

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:107616-56-8 SDS

107616-56-8Downstream Products

107616-56-8Relevant articles and documents

Iododediazoniation of Arenediazonium Salts Accompanied by Aryl Radical Ring Closure

Beckwith, Athelstan L. J.,Meijs, Gordon F.

, p. 1922 - 1930 (2007/10/02)

Treatment of o-(allyloxy)benzenediazonium tetrafluoroborate (1a) with sodium iodide in acetone affords the cyclized iodide 2a in good yield by a mechanism involving the generation and exo cyclization of the aryl radical 6a.Other diazonium salts (1b-i) containing suitable unsaturated side chains behave similarly, but those (1l,1m) in which there is an N-allylsulfonamido group yield mainly products formed by endo cyclization.The diazonium salts 1j and 1k do not give cyclized products.Factors affecting the mechanism, rates, and regiochemistry of the reaction are discussed.

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