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2(5H)-Furanone, 4,5,5-trimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30982-21-9

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30982-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30982-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,8 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30982-21:
(7*3)+(6*0)+(5*9)+(4*8)+(3*2)+(2*2)+(1*1)=109
109 % 10 = 9
So 30982-21-9 is a valid CAS Registry Number.

30982-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,5-trimethyl-3-phenylfuran-2-one

1.2 Other means of identification

Product number -
Other names 4,5,5-trimethyl-3-phenyl-5H-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:30982-21-9 SDS

30982-21-9Downstream Products

30982-21-9Relevant academic research and scientific papers

Application of microwaves in organic synthesis: A rapid and efficient synthesis of new 3-aryl-2-imino-4-methyl-2,5-dihydrofurans and 3-aryl-3-2-(5H)-furanones

Villemin, Didier,Liao, Liang

, p. 1575 - 1585 (2003)

New 3-aryl-2-imino-4-methyl-2,5-dihydrofurans (3a-f) were efficiently synthesized by a one-pot condensation under focused microwave irradiation from simple and readily available starting materials. Hydrolysis of (3a-f) gave 3-aryl-4-methyl-2-(5H)-furanones (4a-f).

Copper-Catalyzed [2 + 3] Cyclization of α-Hydroxyl Ketones and Arylacetonitriles: Access to Multisubstituted Butenolides and Oxazoles

Qi, Chaorong,Peng, Youbin,Wang, Lu,Ren, Yanwei,Jiang, Huanfeng

, p. 11926 - 11935 (2018/09/25)

A copper-catalyzed [2 + 3] formal cyclization reaction between α-hydroxyl ketones and arylacetonitriles has been developed. The reaction outcome was ultimately dependent on the structure of the α-hydroxy ketones employed. Tertiary α-hydroxy ketones gave 3,4,5,5-tetrasubstituted butenolides as the sole products, while secondary α-hydroxy ketones furnished 2,4,5-trisubstituted oxazoles selectively. This method has many advantages, such as the use of easily available substrates, broad substrate scope, good functional tolerance, and milder reaction conditions.

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