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1H-2,3-Benzoxazin-1-one, 4-(3,4-dimethylphenyl)- is a chemical compound belonging to the benzoxazinone class, characterized by a benzene ring fused to an oxazine ring. This specific compound features a 3,4-dimethylphenyl group attached to the 4-position of the benzoxazinone core. It is represented by the chemical formula C12H11NO2 and has a molecular weight of 199.22 g/mol. The compound is known for its potential applications in various fields, including pharmaceuticals and agrochemicals, due to its unique structure and properties.

1855-20-5

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1855-20-5 Usage

Chemical class

Benzoxazinones

Derivative

4-(3,4-dimethylphenyl) substituted benzoxazine

Medicinal properties

Anti-inflammatory and antioxidant effects

Potential applications

Drug development and organic synthesis

Role in nature

Plant defense mechanisms against pests and pathogens

Presence in plants

Found in certain plant species

Scientific and industrial interest

Diverse range of potential uses in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 1855-20-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1855-20:
(6*1)+(5*8)+(4*5)+(3*5)+(2*2)+(1*0)=85
85 % 10 = 5
So 1855-20-5 is a valid CAS Registry Number.

1855-20-5Relevant academic research and scientific papers

Copper-catalysed rearrangement of 4-substituted-2,3-1H-benzoxazine-1-thiones

Agirbas, Hikmet,Guener, Selahattin

, p. 257 - 263 (2000)

4-Substituted-2,3-1H-benzoxazine-1-thiones were prepared by the treatment of the corresponding benzoxazine-1-ones with P2S5. The thermal rearrangement of 4-substituted-2,3-1H-benzoxazine-1-thiones, catalysed by metallic copper, yield

Synthesis of Some 4-Substituted 1H-2,3-Benzoxazin-1-ones

Bansal, R. K.,Kumar, Girijesh,Jain, S. K.,Puri, B. K.

, p. 1045 (2007/10/02)

The title compounds have been prepared by treating the corresponding o-aroylbenzoic acids with hydroxylamine hydrochloride and sodium acetate in ethanol, and their structures established by elemental analyses and spectral data.The mechanism suggested for

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