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4H-Pyran-4-one, 2,3-dihydro-3,5-dimethyl-2-phenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83379-03-7

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83379-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83379-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,7 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83379-03:
(7*8)+(6*3)+(5*3)+(4*7)+(3*9)+(2*0)+(1*3)=147
147 % 10 = 7
So 83379-03-7 is a valid CAS Registry Number.

83379-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2RS,3SR)-3,5-dimethyl-2-phenyl-2,3-dihydro-4H-pyran-4-one

1.2 Other means of identification

Product number -
Other names (2S,3R)-3,5-Dimethyl-2-phenyl-2,3-dihydro-pyran-4-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:83379-03-7 SDS

83379-03-7Downstream Products

83379-03-7Relevant academic research and scientific papers

Diastereo- and enantioselective synthesis of trans-2,3-disubstituted 2,3-dihydropyran-4-one derivatives

Scettri, Arrigo,Acocella, Maria R.,Palombi, Laura,Scalera, Chiara,Villano, Rosaria,Massa, Antonio

, p. 2229 - 2236 (2007/10/03)

trans-Diastereoselective hetero-Diels-Alder reactions took place in the presence of SiCl4/ activator systems. The reactions of aldehydes with a derivative of Danishefsky's diene afforded the corresponding pyrones with high yields and diastereos

Asymmetric Hetero Diels-Alder Reaction Catalyzed by Stable and Easily Prepared CAB Catalyst

Gao, Quingzhi,Ishihara, Kazuaki,Maruyama, Tohru,Mouri, Makoto,Yamamoto, Hisashi

, p. 979 - 988 (2007/10/02)

A stable chiral (acyloxy)borane (CAB) complex is prepared in situ by mixing a tartaric acid derivative and arylboronic acids at room temperature.A solution of the catalyst is effective in catalyzing hetero Diels-Alder reactions to produce dihydropyrone derivatives of high optical purities.

Asymmetric Hetero Diels-Alder Reaction Catalyzed by Stable and Easily Prepared CAB Catalysts

Gao, Qingzhi,Maruyama, Tohru,Mouri, Makoto,Yamamoto, Hisashi

, p. 1951 - 1952 (2007/10/02)

A stable chiral (acyloxy)borane (CAB) complex is prepared in situ by mixing tartaric acid derivative and arylboric acid at room temperature.A solution of the catalyst is effective to catalyze hetero Diels-Alder reaction to produce dihydropyrone derivative

ELECTRONIC AND STERIC EFFECTS OF LEWIS ACIDIC ORGANOALUMINUM REAGENTS IN THE DIELS-ALDER REACTION

Maruoka, Keiji,Nonoshita, Katsumasa,Yamamoto, Hisashi

, p. 1453 - 1460 (2007/10/02)

The influence of electronic and steric effects of modified organoaluminum reagents to the stereoselectivity in the Diels-Alder and hetero-Diels-Alder reactions has been examined.

Chelation-Controlled Facially Selective Cyclocondensation Reactions of Chiral Alkoxy Aldehydes: Syntheses of a Mouse Androgen and of a Carbon-Linked Disaccharide

Danishefsky, Samuel J.,Pearson, William H.,Harvey, Daniel F.,Maring, Clarence J.,Springer, James P.

, p. 1256 - 1268 (2007/10/02)

Magnesium bromide in tetrahydrofuran catalyzes the cycloaddition of a variety of chiral alkoxy aldehydes with activated butadienes.The stereochemistry of these products is such that they can be rationalized as arising from a reacting conformer in which th

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