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2H-Pyran, tetrahydro-2-2-methoxy-4-(2-propenyl)phenoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72066-75-2

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72066-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72066-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72066-75:
(7*7)+(6*2)+(5*0)+(4*6)+(3*6)+(2*7)+(1*5)=122
122 % 10 = 2
So 72066-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-3-6-12-8-9-13(14(11-12)16-2)18-15-7-4-5-10-17-15/h3,8-9,11,15H,1,4-7,10H2,2H3

72066-75-2SDS

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 2-(2-methoxy-4-prop-2-enylphenoxy)oxane

1.2 Other means of identification

Product number -
Other names Eugenol tetrahydropyran

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:72066-75-2 SDS

72066-75-2Downstream Products

72066-75-2Relevant academic research and scientific papers

3,5-Dinitrobenzoic acid catalyzed synthesis of 2,3-unsaturated O- and S-glycosides and tetrahydropyranylation of alcohols and phenols

Bodipati, Naganjaneyulu,Palla, Srinivasa Rao,Komera, Venkateshwarlu,Peddinti, Rama Krishna

, p. 6878 - 6881 (2014)

A simple procedure for the synthesis of 2,3-unsaturated glycosides in acetonitrile and tetrahydropyranylation of alcohols and phenols in dichloromethane in the presence of 3,5-dinitrobenzoic acid is described. A variety of alcohols and thiols are reacted with glycals to give the desired products in high yields with high α-selectivity.

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