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2(3H)-Furanone, dihydro-3-(4-methoxybenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58688-30-5

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58688-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58688-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58688-30:
(7*5)+(6*8)+(5*6)+(4*8)+(3*8)+(2*3)+(1*0)=175
175 % 10 = 5
So 58688-30-5 is a valid CAS Registry Number.

58688-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxybenzoyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 3-(4-methoxy-benzoyl)-dihydro-furan-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:58688-30-5 SDS

58688-30-5Relevant academic research and scientific papers

A palladium-catalyzed asymmetric allylic alkylation approach to α-quaternary γ-butyrolactones

De Oliveira, Marllon Nascimento,Fournier, Jeremy,Arseniyadis, Stellios,Cossy, Janine

supporting information, p. 14 - 17 (2017/11/27)

The Pd-catalyzed asymmetric allylic alkylation (Pd-AAA) of enol carbonates derived from γ-butyrolactones is reported, affording the corresponding enantioenriched α,α′-disubstituted γ-butyrolactones in both high yields and high enantioselectivities (up to 94% ee). This method was eventually applied to the synthesis of chiral spirocyclic compounds.

Enantioselective ketone hydroacylation using noyori's transfer hydrogenation catalyst

Murphy, Stephen K.,Dong, Vy M.

supporting information, p. 5553 - 5556 (2013/05/22)

An enantioselective ketone hydroacylation enables the direct preparation of lactones from keto alcohols. The alcohol is oxidized in situ to an aldehyde, obviating the need to prepare sensitive keto aldehyde substrates. Noyori's asymmetric transfer hydroge

Unexpected reaction of a dimethylzinc-generated THF radical with aldehydes

Yamamoto, Yasutomo,Yamada, Ken-Ichi,Tomioka, Kiyoshi

, p. 795 - 797 (2007/10/03)

A dimethylzinc-air-generated THF radical reacted with aldehydes at the β-position of an α-oxygenated THF.

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