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The chemical "2-Propenoic acid, 3-(1,4-dioxaspiro[4.5]dec-7-en-7-yl)-, methyl ester, (2E)-" is a complex organic compound with the molecular formula C9H12O5. It is a derivative of 2-propenoic acid, featuring a methyl ester group and a 1,4-dioxaspiro[4.5]dec-7-en-7-yl moiety. The "2E" notation indicates that the molecule has a specific geometric configuration, with the double bond in the E (entgegen) configuration. 2-Propenoic acid, 3-(1,4-dioxaspiro[4.5]dec-7-en-7-yl)-, methyl ester, (2E)- is characterized by its unique structure, which includes a spiro ring system and a diene functionality, making it a potentially interesting molecule for various applications in organic chemistry and material science.

226916-17-2

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226916-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226916-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 226916-17:
(8*2)+(7*2)+(6*6)+(5*9)+(4*1)+(3*6)+(2*1)+(1*7)=142
142 % 10 = 2
So 226916-17-2 is a valid CAS Registry Number.

226916-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,4-dioxaspiro[4.5]dec-7-en-7-yl)acrylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

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

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More Details:226916-17-2 SDS

226916-17-2Upstream product

226916-17-2Relevant academic research and scientific papers

PREPARATION OF CHIRAL PROPARGYLIC ALCOHOL AND ESTER INTERMEDIATES OF HIMBACINE ANALOGS

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Page/Page column 42, (2008/06/13)

This application discloses a novel process for the conversion of a series of racemic propargylic alcohols to corresponding (R)-enantiomers. The application also discloses the enantio-selective esterification of a propargylic alcohol from its racemate to p

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