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101833-09-4

5-methyl-3-phenyl-3-(prop-2-en-1-yl)dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101833-09-4

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101833-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101833-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,8,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101833-09:
(8*1)+(7*0)+(6*1)+(5*8)+(4*3)+(3*3)+(2*0)+(1*9)=84
84 % 10 = 4
So 101833-09-4 is a valid CAS Registry Number.

101833-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-3-phenyl-3-prop-2-enyloxolan-2-one

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-phenyl-4-allyltetrahydrofuranone-5

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:101833-09-4 SDS

101833-09-4Downstream Products

101833-09-4Relevant articles and documents

Combined dealkoxycarbonylation and lactonisation of unsaturated malonates in ionic liquids

Oswald, Magalie F.,Parsons, Andrew F.,Yang, Wei,Bowden, Martin

, p. 8087 - 8089 (2005)

Heating unsaturated malonates with LiCl and water in [bmim][Br] or [bmim][BF4]/[bmim][Br] produces unsaturated esters or lactones, respectively.

Triflic acid mediated dealkylative lactonisation via NMR-observable alkyloxonium intermediates

Munoz, M. Paz,Lloyd-Jones, Guy C.

experimental part, p. 516 - 524 (2009/07/19)

Trifluoromethanesulfonic acid (TfOH) efficiently induces the dealkylative cyclisation of pent-4-enoates to generate γ-lac-tones with high selectivity. For primary alkyl esters bearing an additional alkene, only monolactonisation occurs, even in the presen

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