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1,3-Propanedione, 2-[(dimethylamino)methylene]-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85302-05-2

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85302-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85302-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,0 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85302-05:
(7*8)+(6*5)+(5*3)+(4*0)+(3*2)+(2*0)+(1*5)=112
112 % 10 = 2
So 85302-05-2 is a valid CAS Registry Number.

85302-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylaminomethylidene)-1,3-diphenylpropane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-[(dimethylamino)methylene]-1,3-diphenyl-1,3-propanedione

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:85302-05-2 SDS

85302-05-2Relevant articles and documents

The synthesis of ethyl 2-[(2,2-dibenzoyl)ethenyl]amino-3- dimethylaminopropenoate and its application to the synthesis of fused 3- aminopyran-2-ones and 3-aminoazolo- and -azinopyrimidin-4(4H)-ones

Sorsak, Gorazd,Grdadolnik, Simona Golic,Stanovnik, Branko

, p. 1275 - 1279 (1998)

Ethyl 2-[(2,2-dibenzoyl)ethenyl]amino-3-dimethylaminopropenoate (3) was prepared from dibenzoylmethane (1) in two steps, and used as a reagent for preparation of fused substituted 3-aminopyranones 12-15 in over 90% yield, quinolizin-4-one 16 in over 79% y

Synthesis of 4-aroyl-5-arylpyrazoles and 4-aroyl-3-arylpyrazoles via the reaction of enaminodiketones with substituted hydrazines

Choshi, Tominari,Hatae, Noriyuki,Hibino, Satoshi,Kotouge, Rika,Nishiyama, Takashi,Oikawa, Tsutomu,Ono, Kanako,Yamauchi, Akira

, p. 25 - 45 (2020/01/28)

Pyrazole is a five-membered heterocyclic compound and is one of the important heterocycles in the fields of medicine and pharmacology. Here, we demonstrate the reactivity of symmetrical enaminodiketones 8–14 with substituted hydrazines. When using alkylhy

SUBSTITUTED ENAMINONES, THEIR DERIVATIVES AND USES THEREOF

-

Page/Page column 37-38, (2008/06/13)

The invention relates to substituted enaminones of Formula (I) and their derivatives and the discovery that these compounds modulate the effect of γ-aminobutyric acid (GABA) on the GABAA receptor complex in a therapeutically relevant fashion and may be us

Reaction of 2-Dimethylaminomethylene-1,3-diones with Dinucleophiles. I. Synthesis of 1,5-Disubstituted 4-Acylpyrazoles

Schenone, Pietro,Mosti, Luisa,Menozzi, Giulia

, p. 1355 - 1361 (2007/10/02)

Reaction of open-chain and cyclic sym-1,3-diones with N,N-dimethylformamide dimethyl acetal gave, generally in high yield, a series of sym-2-dimethylaminomethylene-1,3-diones which reacted with phenylhydrazine and methylhydrazine to afford, generally in satisfactory yield, a number of 1,5-disubstituted 4-acylpyrazoles.The applications and limits of this new pyrazole synthesis are presented and discussed.

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