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Spiro[bicyclo[2.2.1]hept-2-ene-7,2-[1,3]dioxolane] is a complex organic chemical compound characterized by a unique spiro structure, which consists of two rings sharing a common atom. The compound features a bicyclo[2.2.1]hept-2-ene ring, which is a seven-membered ring with two carbon-carbon double bonds, and a 1,3-dioxolane ring, which is a five-membered ring containing two oxygen atoms. This spiro compound is known for its potential applications in various chemical and pharmaceutical industries, as well as its intriguing structural properties that make it a subject of interest for researchers in organic chemistry.

1491-12-9

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1491-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1491-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1491-12:
(6*1)+(5*4)+(4*9)+(3*1)+(2*1)+(1*2)=69
69 % 10 = 9
So 1491-12-9 is a valid CAS Registry Number.

1491-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name spiro[1,3-dioxolane-2,7'-bicyclo[2.2.1]hept-2-ene]

1.2 Other means of identification

Product number -
Other names 2-norbornen-7-one ethylene acetal

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:1491-12-9 SDS

1491-12-9Relevant academic research and scientific papers

Enantioselective synthesis of (-)-curcumanolide A using enzymatic transesterification of meso-spirodiol

Fujita, Toshiaki,Tanaka, Masakazu,Norimine, Yoshihiko,Suemune, Hiroshi,Sakai, Kiyoshi

, p. 3824 - 3830 (1997)

meso-Spirodiol 12 and spirodiacetate 13 were stereoselectively prepared using π-face selective Grignard addition to norbornanone 7. Asymmetric transesterification of meso-diol and hydrolysis of meso-diacetate were studied using lipases. Pseudomonas fluorescens lipase-catalyzed transesterification of meso-diol 12 afforded the monoacetate (-)-21 of high enantiomeric excess (> 99% ee). The formal synthesis of (-)-curcumanolide A has been achieved from the optically active (-)-21.

HEPATITIS C VIRUS INHIBITORS

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Page/Page column 74-75, (2012/03/09)

The present disclosure relates to compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment o

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