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60212-12-6

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60212-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60212-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,1 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60212-12:
(7*6)+(6*0)+(5*2)+(4*1)+(3*2)+(2*1)+(1*2)=66
66 % 10 = 6
So 60212-12-6 is a valid CAS Registry Number.

60212-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-2-phenyl-2-methyl-2-ethanol

1.2 Other means of identification

Product number -
Other names 12-Jod-11-oxy-1-isopropyl-benzol

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:60212-12-6 SDS

60212-12-6Relevant articles and documents

Reaction of trifluoromethanesulfonamide with alkenes and cycloocta-1,5-diene under oxidative conditions. Direct assembly of 9-heterobicyclo[4.2.1]nonanes

Moskalik,Shainyan,Schilde

, p. 1271 - 1277 (2011)

Reactions of trifluoromethanesulfonamide with α-methylstyrene, 2-methylpent-1-ene, and cycloocta-1,5-diene in the system t-BuOCl-NaI were studied. In the reaction with α-methylstyrene 1-iodo-2-phenylpropan-2-ol was the only isolated product. The reaction

Regio- and stereoselective co-iodination of olefins using NH4I and Oxone

Durgaiah, Chevella,Naresh, Mameda,Arun Kumar, Macharla,Swamy, Peraka,Reddy, Marri Mahender,Srujana, Kodumuri,Narender, Nama

supporting information, p. 1133 - 1144 (2016/07/22)

A simple, efficient, and environmentally benign protocol for the synthesis of vicinal iodohydrins and iodoesters from olefins using NH4I and Oxone in CH3CN/H2O (1:1) and dimethylformamide (DMF) / dimethylacetamide (DMA), respectively, without employing a catalyst at room temperature is described. Regio- and stereoselective iodohydroxylation and iodoesterification of various olefins with anti fashion, following Markonikov’s rule, was achieved and the corresponding products were obtained in good to excellent yields. In addition, 1,2-disubstituted olefins afforded excellent diastereoselectivity.

Benzyl(triphenyl)phosphonium Dichloroiodate: A New Reagent for Coiodination of Alkenes

Alikarami, Mohammad,Farhadi, Mansoureh

, p. 1302 - 1306 (2015/09/22)

A mild, efficient, and regio- and stereoselective method for iodoalkoxylation and iodohydroxylation of olefins has been developed using benzyl(triphenyl)phosphonium dichloroiodate as iodine source. This procedure led to the corresponding iodoalkoxylated and iodohydroxylated products in moderate to excellent yields.

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