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Product Name:(3aR,4R,7R,7aS)-3a,4,7,7a-Tetrahydro-4,7-ethanoisobenzofuran-1,3-dione

IUPAC Name:(1R,2R,6S,7R)-4-oxatricyclo[5.2.2.02,?]undec-8-ene-3,5-dione

CAS:24327-08-0
Molecular Formula:C10H10O3
Purity:95%
Catalog Number:CM203192
Molecular Weight:178.19

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CM203192-5g in stock ???

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Product Details

CAS NO:24327-08-0
Molecular Formula:C10H10O3
Melting Point:-
Smiles Code:O=C1OC([C@]2([H])[C@@]3([H])C=C[C@](CC3)([H])[C@@]21[H])=O
Density:
Catalog Number:CM203192
Molecular Weight:178.19
Boiling Point:340.9°C at 760 mmHg
MDL No:MFCD00151124
Storage:Store at 2-8°C.

Category Infos

Bridged Compounds
Bridged ring compound refers to any two rings in the compound, which share two non-directly connected carbon atoms, and are classified into bicyclic hydrocarbons, tricyclic hydrocarbons, tetracyclic hydrocarbons, etc. Carbon atoms used in two or more rings are bridgehead carbon atoms, and the bond connecting the bridgehead carbon atoms is called a bridge. Bridged ring compounds are a class of organic compounds that are widely present in nature and usually have important physiological activities, such as the famous anticancer drug paclitaxel and antimalarial drug artemisinin.
bridged compounds,bridged bicyclic compounds
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Cyclohexanes
Cyclohexane is an organic compound with a chemical formula C6H12. It is a colorless liquid with a pungent odor, insoluble in water, and soluble in most organic solvents such as ethanol, ether, benzene, and acetone. Cyclohexyl fragments are a common structure in both natural and synthetic drugs. It can be used as both core structure and part of achiral side chain.
Tetrahydrofurans
Tetrahydrofuran is a heterocyclic organic compound with the molecular formula C4H8O. Tetrahydrofuran belongs to ethers and is the complete hydrogenation product of furan. It is a colorless, water-miscible organic liquid with small viscosity at normal temperature and pressure. Because of its long liquid range, it is a commonly used medium polar aprotic solvent. Its main use is as a precursor of high molecular polymers.
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