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4H-3,1-Benzoxazin-4-one, 1-(2,3-dimethylphenyl)-1,2-dihydro- is a complex organic compound belonging to the benzoxazinone family. It is characterized by a benzoxazinone core, which consists of a benzene ring fused to an oxazinone ring. The compound features a 2,3-dimethylphenyl group attached to the benzoxazinone core, which introduces two methyl groups at the 2nd and 3rd carbon positions of the phenyl ring. This specific arrangement of atoms and functional groups gives the compound unique chemical and physical properties, making it a potential candidate for various applications in the fields of chemistry, pharmaceuticals, and materials science.

1804-54-2

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1804-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1804-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1804-54:
(6*1)+(5*8)+(4*0)+(3*4)+(2*5)+(1*4)=72
72 % 10 = 2
So 1804-54-2 is a valid CAS Registry Number.

1804-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1',2'-dimethyl-phenyl)-1,2-dihydro-3,1-benzoxazin-4-one

1.2 Other means of identification

Product number -
Other names (dimethyl-2,3 phenyl)-1 dihydro-1,2 benzoxazine-3,1 one-4

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:1804-54-2 SDS

1804-54-2Relevant academic research and scientific papers

COMPOSES SULFURES HETEROCYCLIQUES. XCVI. REACTION DE L'HYDRAZINE SUR LES DIHYDRO-1,2 BENZOTHIAZINE-3,1 THIONES-4

Legrand, Louis,Lozac'H, Noel

, p. 139 - 143 (2007/10/02)

1-Alkyl-1,2-dihydro-3,1-benzothiazine-4-thiones 1, when reacting with hydrazine, give with a good yield a 1-alkyl-3-amino-2,3-dihydro-1H-quinazoline-4-thione-2, often together with a derivative of 1,3,4-thiadiazole-3. With 1-aryl-1,2-dihydro-3,1-benzothiazine-4-thiones, the main product of the reaction with hydrazine appears to be a 1-aryl-4-hydrazono-1,4-dihydro-2H-3,1-benzothiazine 4, sometimes with some amount of 3.On the contrary, when reacting with hydrazine, 1-alkyl (or 1-aryl)-1,2-dihydro-3,1-benzothiazin-4-ones lead to a 2-alkylamino (or arylamino)-benzohydrazide 5. By thermolysis 4 isomerizes into 2 which is accompanied by derivatives (3 and 7) of 1,3,4-thiadiazole.The structures of compounds 2, 4 and 7 have been studied by NMR and UV spectrometry.

New esters of N arylanthranilic acids

Salimbeni,Manghisi,Magistretti

, p. 276 - 286 (2007/10/06)

A series of acyloxy and alkyloxymethyl esters of meclofenamic, flufenamic and mefenamic acids has been synthesized and its antiinflammatory, analgesic and antipyretic activities have been compared with those of the corresponding acids and the methyl, β,γ isopropylidenedioxypropyl, and N,N diethylaminoethyl esters. The acyloxy and alkyloxymethyl esters are the most interesting compounds, because they possess pharmacological activity of the same order as that of the corresponding acids and a lower toxicity. The ethoxymethyl ester of N (2,6 dichloro m tolyl)anthranilic acid is presently under clinical investigation.

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