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33447-73-3

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33447-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33447-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,4 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33447-73:
(7*3)+(6*3)+(5*4)+(4*4)+(3*7)+(2*7)+(1*3)=113
113 % 10 = 3
So 33447-73-3 is a valid CAS Registry Number.

33447-73-3SDS

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 phthalic acid mono-(1-methyl-allyl ester)

1.2 Other means of identification

Product number -
Other names Phthalsaeure-mono-(1-methyl-allylester)

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:33447-73-3 SDS

33447-73-3Downstream Products

33447-73-3Relevant articles and documents

Chiral 2,2-Disubstituted Cyclohexanones; Annulation via Claisen Rearrangement Products

Grattan, T. J.,Whitehurst, J. S.

, p. 11 - 18 (2007/10/02)

The methyl enol ether of 2-methylcyclohexanone reacts regiospecifically with the optical active forms of but-3-yn-2-ol and but-3-en-2-ol. (R)-But-3-yn-2-ol yields an approximately 4:1 mixture of (R)-2-methyl-2-(R-buta-1,2-dienyl)cyclohexanone and the corresponding SR compound.By contrast the but-3-en-2-ol reaction is ca. 96percent enantioselective; (R)-but-3-en-2-ol gives (R)-2-(trans-but-2-enyl)-2-methylcyclohexanone and (S)-but-3-en-2-ol gives the corresponding (S)-cyclohexanone.These Claisen rearrangement products have been transformed into Robinson-type annulated ketones.Cleavage of some highly hindered esters has been carried out efficiently by sodium methylsulphinyl-methanide in dimethyl sulphoxide.

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