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Oxetane, 2,2-dimethoxy-3-methyl-4-phenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62841-80-9

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62841-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62841-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,4 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62841-80:
(7*6)+(6*2)+(5*8)+(4*4)+(3*1)+(2*8)+(1*0)=129
129 % 10 = 9
So 62841-80-9 is a valid CAS Registry Number.

62841-80-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-2,2-dimethoxy-3-methyl-4-phenyloxetane

1.2 Other means of identification

Product number -
Other names Oxetane,2,2-dimethoxy-3-methyl-4-phenyl-,trans

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:62841-80-9 SDS

62841-80-9Relevant academic research and scientific papers

Chemistry of Ketene Acetals. Part 8. Stereochemistry of the Reaction of 1,1-Dimethoxypropene with Aldehydes

Hofstraat, Rob G.,Scheeren, Hans W.,Nivard, Rutger J. F.

, p. 561 - 564 (2007/10/02)

The Lewis acid-catalysed (2+2)cycloadditions of 1,1-dimethoxypropene with various aldehydes RCHO have been studied.These reactions, which are supposed to proceed via dipolar intermediates, yield 2,2-dimethoxyoxetanes, the formation of which is reversible

HIGH PRESSURE PROMOTED (2+2) CYCLOADDITIONS OF KETENE ACETALS WITH CARBONYL COMPOUNDS

Aben, Rene W. M.,Scheeren, Hans W.

, p. 4613 - 4616 (2007/10/02)

Cycloadditions of ketene acetals (R1R2C=C(OR)2) with carbonyl compounds (R3COR4) are strongly promoted by increase of pressure.At 12 kbar oxetanes are even obtained from very polar ketene acetals (R1,

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