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

185347-49-3

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185347-49-3 Usage

Molecular Weight

184.20

Chemical Family

Furanone

Usage

Commonly used in the fragrance and flavor industry.

Odor Description

Sweet, caramel-like odor.

Applications

Often used in perfumes, body care products, and food flavorings.

Potential Applications

Studied for its potential as an anti-quorum sensing agent, meaning it may have applications in inhibiting bacterial communication and biofilm formation.

Check Digit Verification of cas no

The CAS Registry Mumber 185347-49-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185347-49:
(8*1)+(7*8)+(6*5)+(5*3)+(4*4)+(3*7)+(2*4)+(1*9)=163
163 % 10 = 3
So 185347-49-3 is a valid CAS Registry Number.

185347-49-3SDS

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-(2-methoxyphenyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names -

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:185347-49-3 SDS

185347-49-3Downstream Products

185347-49-3Relevant academic research and scientific papers

Weak arene C-h×××o hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones

Huang, Zhiyan,Chen, Zuliang,Lim, Li Hui,Quang, Gia Chuong Phan,Hirao, Hajime,Zhou, Jianrong

supporting information, p. 5807 - 5812 (2013/07/05)

Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH×××O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH×××O hydrogen bonding to guide stereoselection. Copyright

A thermal rearrangement of ethylene acetal of bicyclo[4.2.0]octa-4,7-diene-2,3-dione

Oda, Mitsunori,Kamata, Yoshitaka,Nishii, Satoshi,Miyatake, Ryuta,Kuroda, Shigeyasu,Oda, Masaji

, p. 445 - 446 (2007/10/03)

Pyrolysis of the title compound 3 at 400°C gave α-(2-hydroxyphenyl)-γ-butyrolactone (4) whose structure was confirmed by an alternative synthesis. A reaction mechanism via a phenyl ketene acetal is proposed.

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