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3-Oxabicyclo[3.1.0]hexane-2,4-dione, 1-phenyl-, also known as 1-phenyl-3-oxabicyclo[3.1.0]hexane-2,4-dione, is a chemical compound with the molecular formula C9H8O3. It is a derivative of 3-oxabicyclo[3.1.0]hexane-2,4-dione, featuring a phenyl group attached to the 1-position. 3-Oxabicyclo[3.1.0]hexane-2,4-dione, 1-phenyl- is characterized by its bicyclic structure, with a six-membered ring containing an oxygen atom and a five-membered ring. The presence of the phenyl group introduces aromaticity and additional steric hindrance to the molecule. 3-Oxabicyclo[3.1.0]hexane-2,4-dione, 1-phenyl- may be of interest in organic chemistry, potentially serving as an intermediate in the synthesis of more complex molecules or as a building block in materials science. Its specific applications and properties would depend on the context in which it is used, and further research would be needed to explore its potential uses and reactivity.

710-97-4

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710-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 710-97-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 710-97:
(5*7)+(4*1)+(3*0)+(2*9)+(1*7)=64
64 % 10 = 4
So 710-97-4 is a valid CAS Registry Number.

710-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-oxabicyclo[3.1.0]hexane-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-phenyl-cyclopropane-1,2-dicarboxylic acid anhydride

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:710-97-4 SDS

710-97-4Relevant academic research and scientific papers

Furan-2(3H)- and -2(5H)-ones. Part 6. Di-?-methane rearrangement of the α-substituted 4-benzylfuran-2(5H)-one system

Muraoka, Osamu,Tanabe, Genzoh,Higachiura, Mie,Minematsu, Toshie,Momose, Takefumi

, p. 1437 - 1444 (2007/10/02)

The effect of the 'central methane' substitution on the di-?-methane rearrangement in 4-benzyl-2,5-dihydrofuran-2-ones 8a-d was investigated.Significant enhancement of efficiency in the rearrangement leading in high combined yields to two isomeric products, endo-12 and exo-12, is discussed in terms of both the substituent effects at the benzylic carbon and the restrained features of the ring-enrolled ?-system.The origin of the difference in chemoselectivity compared with that of the 3-benzyl counterpart 5 where a photoarylated product 6 resulted upon photoirradiation was also investigated, and was rationalized by postulating a higher reactivity at the β-position of the enone system.

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