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7-(diethylamino)-4-methyl-3-phenyl-2H-chromen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29197-96-4

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29197-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29197-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29197-96:
(7*2)+(6*9)+(5*1)+(4*9)+(3*7)+(2*9)+(1*6)=154
154 % 10 = 4
So 29197-96-4 is a valid CAS Registry Number.

29197-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(diethylamino)-4-methyl-3-phenylchromen-2-one

1.2 Other means of identification

Product number -
Other names 7-diethylamino-4-methyl-3-phenyl-chromen-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:29197-96-4 SDS

29197-96-4Downstream Products

29197-96-4Relevant academic research and scientific papers

Regioselective C-3 arylation of coumarins with arylhydrazines via radical oxidation by potassium permanganate

Yuan, Jin-Wei,Li, Wei-Jie,Yang, Liang-Ru,Mao, Pu,Xiao, Yong-Mei

, p. 1115 - 1123 (2016/11/16)

An efficient protocol for oxidative C-3 arylation of coumarins with arylhydrazine has been developed using potassium permanganate as an oxidant. The arylated coumarins with different electronic properties were obtained in moderate to good yields. The deve

PHOTOCHEMICAL REACTIONS OF 7-AMINOCOUMARINS. 8. REACTION OF 3-IODO-4-METHYL-7-DIETHYLAMINOCOUMARIN WITH MONOSUBSTITUTED BENZENES

Gordeeva, N. A.,Kirpichenok, M. A.,Gernyshev, A. I.,Grandberg, I.I.,Akimova, N. P.

, p. 976 - 980 (2007/10/02)

A number of 3-aryl-4-methyl-7-diethylaminocoumarins were obtained as a result of the photolysis of 3-iodo-4-methyl-7-diethylaminocoumarin in the presence of benzene, chlorobenzene, fluorobenzene, benzonitrile, toluene, and diphenyl ether.On the basis of an analysis of the PMR spectra it was established that photosubstitution leads to o- and p-isomeric products.The mechanism of the reaction was studied.

PHOTOCHEMICAL REACTIONS OF 7-AMINOCOUMARINS. 6. REACTION OF 7-DIALKYLAMINOCOUMARINS WITH HALO DERIVATIVES

Kirpichenok, M. A.,Mel'nikova, L. M.,Denisov, L. K.,Grandberg, I. I.

, p. 858 - 862 (2007/10/02)

3-Substituted 7-dialkylaminocoumarins were synthesized as a result of the photoreaction of 7-diethylaminocoumarin, 4-trifluoromethyl-7-diethylaminocoumarin, 4-chloro-7-diethylaminocoumarin, 4-(N-morpholino)-7-diethylaminocoumarin, and coumarin-102 (2,3,6,

PHOTOCHEMICAL REACTIONS OF 7-AMINOCOUMARINS. 4. REACTION OF 4-METHYL-7-DIETHYLAMINOCOUMARIN WITH COMPOUNDS TENDING TO PHOTOLYTIC DISSOCIATION

Kirpichenok, M. A.,Mel'nikova, L. M.,Denisov, L. K.,Grandberg, I. I.

, p. 380 - 388 (2007/10/02)

The photochemical reactions of 4-methyl-7-diethylaminocoumarin with a series of alkyl halides including isopropyl iodide, allyl iodide, bromoacetone, α-bromoethyl acetate, phenacyl bromide, p-bromophenacyl bromide, and chloroacetonitrile, and aryl iodides including iodobenzene, 2-nitroiodobenzene, 3,4-dimethoxyiodobenzene, and 3-iodo-4-methyl-7-diethylaminocoumarin proceed by a radical addition mechanism to give 3-substituted aminocoumarins.A series of 3-substituted 7-aminocoumarins was also obtained as a result of the photochemical reactions of 4-methyl-7-diethylaminocoumarin, with other reagents, having photolabile chemical bonds such as dioxanyl peroxide, phenyl iodosodiacetate, and nitromethane.The luminescence characteristics of the compounds synthesized were studied.

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