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82027-15-4

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82027-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82027-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,2 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82027-15:
(7*8)+(6*2)+(5*0)+(4*2)+(3*7)+(2*1)+(1*5)=104
104 % 10 = 4
So 82027-15-4 is a valid CAS Registry Number.

82027-15-4SDS

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 methyl α-methanesulphonyloxybenzeneacetate

1.2 Other means of identification

Product number -
Other names methyl 2-phenyl-2-(mesyloxy)acetate

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:82027-15-4 SDS

82027-15-4Relevant articles and documents

Iron-Catalyzed Synthesis of Sulfur-Containing Heterocycles

Bosset, Cyril,Lefebvre, Gauthier,Angibaud, Patrick,Stansfield, Ian,Meerpoel, Lieven,Berthelot, Didier,Guérinot, Amandine,Cossy, Janine

, p. 4020 - 4036 (2017/04/27)

An iron-catalyzed synthesis of sulfur- and sulfone-containing heterocycles is reported. The method is based on the cyclization of readily available substrates and proceeded with high efficiency and diastereoselectivity. A variety of sulfur-containing heterocycles bearing moieties suitable for subsequent functionalization are prepared. Illustrative examples of such postcyclization modifications are also presented.

Reaction of benzene and benzene with Trimethylsilyl Enol Ethers. A New General Method for α-Sulfonyloxylation of Carbonyl Compounds

Moriarty, Robert M.,Penmasta, Raju,Awasthi, Alok K.,Epa, W. Ruwan,Prakash, Indra

, p. 1101 - 1104 (2007/10/02)

Reaction of benzene (1) with trimethylsilyl enol ethers of aromatic ketones 4a-d, alicyclic ketone 7, aliphatic ketone 10, and esters 13a-c in dichloromethane at room temperature gives good yields of α-(tosyloxy)carbonyl compounds 5

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