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7129-41-1

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7129-41-1 Usage

General Description

6-oxabicyclo[3.1.0]hex-3-ene, also known as 3,4-epoxy-1,2,3,6-tetrahydrobenzo[c]furan, is a bicyclic compound containing a ring structure with six carbon atoms and one oxygen atom. It is classified as an epoxide, which is a type of organic compound with a unique three-membered ring containing two carbon atoms and one oxygen atom. The compound is commonly used in organic synthesis as a versatile building block for creating various types of complex molecules. It is also of interest in the field of medicinal chemistry and drug development due to its potential pharmacological properties. The compound's unique structure and reactivity make it an important chemical reagent in many different areas of research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 7129-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7129-41:
(6*7)+(5*1)+(4*2)+(3*9)+(2*4)+(1*1)=91
91 % 10 = 1
So 7129-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H6O/c1-2-4-5(3-1)6-4/h1-2,4-5H,3H2

7129-41-1SDS

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 6-oxabicyclo[3.1.0]hex-2-ene

1.2 Other means of identification

Product number -
Other names (+/-)-cyclopentadiene monoepoxide

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:7129-41-1 SDS

7129-41-1Relevant articles and documents

Mild metal-free syn-stereoselective ring opening of activated epoxides and aziridines with aryl borates

Pineschi, Mauro,Bertolini, Ferruccio,Haak, Robert M.,Crotti, Paolo,Macchia, Franco

, p. 1426 - 1428 (2007/10/03)

A conceptually new, simple and practical method for the syn-nucleophilic displacement of aryl and vinyl epoxides and aryl aziridines with (substituted) phenols, using aryl borates as activating nucleophiles under neutral conditions, is reported. The Royal Society of Chemistry 2005.

Substituted alkoxy carbonyl-3-oxo-α-phthalimido-5-isoxozolidineacetic acids

-

, (2008/06/13)

Analogs of tricholomic acids and process for preparing them.

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