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3-Methylhexahydrobenzofuran-2(3H)-one is an organic compound with the molecular formula C8H13NO2. It is a heterocyclic compound, specifically a benzofuran derivative, which features a benzene ring fused to a furan ring. The compound has a methyl group attached to the third carbon of the hexahydrobenzofuran structure, and a ketone functional group at the second position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Due to its complex structure and functional groups, 3-methylhexahydrobenzofuran-2(3H)-one is a subject of interest in organic chemistry research and development.

2205-25-6

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2205-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2205-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2205-25:
(6*2)+(5*2)+(4*0)+(3*5)+(2*2)+(1*5)=46
46 % 10 = 6
So 2205-25-6 is a valid CAS Registry Number.

2205-25-6SDS

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 3-methyl-3a,4,5,6,7,7a-hexahydro-3H-1-benzofuran-2-one

1.2 Other means of identification

Product number -
Other names 3-methyl-hexahydro-benzofuran-2-one

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:2205-25-6 SDS

2205-25-6Relevant academic research and scientific papers

Diastereoselective osmylation and hydroboration of β,γ-unsaturated n,n-diisopropylamides and acid-catalyzed conversion to δ-lactones

Vedejs,Kruger

, p. 4790 - 4797 (2007/10/03)

The title reactions of β,γ-unsaturated N,N-diisopropylamides occur with useful diastereofacial selectivity. The major diol isomer from osmylation of alkenes 1, 10, 11, and 12 in the presence of TMEDA at -78 °C corresponds to the facial preference shown in transition state model 41 (R(z) = H), while the opposite preference for 42 is observed with the Z-alkene 13. (Table 1). Hydroboration with 9-BBN does not show this inversion of diastereofacial selectivity for the Z-alkene. All of the results in Table 2 correspond to the usual preference for a transition state such as 45. Acid- catalyzed lactonization of the alcohols obtained in Tables 1 and 2 can be carried out with overall retention of configuration to afford δ-lactones. Butenolide 5 was prepared with 90% ee from alcohol 2a via osmylation followed by acid-catalyzed lactonization to 3 and elimination using SOCl2/pyridine.

The First Stereoselective Palladium-Catalyzed Cyclocarbonylation of β,γ-Substituted Allylic Alcohols

Brunner, Melanie,Alper, Howard

, p. 7565 - 7568 (2007/10/03)

β,γ-Substituted allylic alcohols react with CO in the presence of catalytic quantities of palladium acetate and 1,4-bis(diphenylphosphino)butane affording α,β-substituted-γ-butyrolactones in 42-85% isolated yields. The complete stereoselectivity observed

Formation of Carbon-Carbon Bonds by Ring Closure of β-Phenylselenocrotonates

Clive, Derrick L. J.,Beaulieu, Pierre L.

, p. 307 - 309 (2007/10/02)

Successive treatment of olefins with PhSeCl and silver crotonate affords β-phenylselenocrotonates which, on reaction with triphenyltin hydride in the presence of azobisisobutyronitrile, are converted into γ-lactones by a process that introduces a new carbon-carbon bond.

A New Approach for Stereoselective Synthesis of γ-Butyrolactones

Ito, Yoshihiko,Kato, Hidehito,Saegusa, Takeo

, p. 741 - 743 (2007/10/02)

Diethylaluminum chloride promotes 1,4-cycloaddition of α,β-unsaturated carbonyl compounds with isocyanides to afford unsaturated N-substituted iminolactones, which are stereoselectively converted to γ-butyrolactones via hydrogenation on Pd/C and then acid

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