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10H-Phenoxazine-1-carboxaldehyde is an organic compound with the chemical formula C11H9NO and a molecular weight of 171.20 g/mol. It is a derivative of phenoxazine, a heterocyclic aromatic compound containing nitrogen and oxygen atoms. This aldehyde is characterized by its yellow crystalline appearance and is soluble in common organic solvents such as ethanol, methanol, and acetone. 10H-Phenoxazine-1-carboxaldehyde is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, dyes, and other organic compounds. It is also known for its fluorescence properties, which can be exploited in the development of sensors and imaging agents. Due to its reactivity, it is essential to handle 10H-Phenoxazine-1-carboxaldehyde with care, following proper safety protocols to minimize potential health and environmental risks.

1918-34-9

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1918-34-9 Usage

Type of compound

Heterocyclic compound

Contains

Phenoxazine group (tricyclic aromatic ring system)

Functional group

Carboxaldehyde

Applications

a. Materials science
b. Organic synthesis
c. Pharmaceutical research

Used as

a. Building block in the synthesis of various organic compounds
b. Fluorescent probe in biological and material science research

Unique properties

a. Chemical structure
b. Reactivity
c. Aromatic properties

Check Digit Verification of cas no

The CAS Registry Mumber 1918-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1918-34:
(6*1)+(5*9)+(4*1)+(3*8)+(2*3)+(1*4)=89
89 % 10 = 9
So 1918-34-9 is a valid CAS Registry Number.

1918-34-9Downstream Products

1918-34-9Relevant academic research and scientific papers

Cycloheptabenzoxazines 3. The Reaction of 6-Bromocycloheptabenzoxazine with o-Aminophenol

Nozoe, Tetsuo,Okai, Harue,Wakabayashi, Hidetsugu,Ishikawa, Sumio

, p. 2307 - 2314 (2007/10/02)

The reaction of 6-bromocycloheptabenzoxazine (19) and o-aminophenol (3) was studied and compared with that of 3-bromo-2-methoxytropone (2) with 3. 14H-Benzoxazinocycloheptabenzoxazine, 10-(o-hydroxyanilino)cycloheptabenzoxazine (D), 1- and 4-formylphenoxazines and their Schiff bases (C and X) were obtained in very good yields by modifying the conditions of the reaction of 19 with 3.Structures of D, C, and their isomers were determined and the possible reaction pathways for the formation of various products are discussed.

A NOVEL SYNTHESIS OF CYCLOHEPTADIBENZOXAZINES AND 14HBENZOXAZINOCYCLOHEPTABENZOXAZINES

Nozoe, Tetsuo,Okai, Harue,Wakabayashi, Hidetsugu,Ishikawa, Sumio

, p. 1145 - 1148 (2007/10/02)

The title compounds, namely, the chiral acetals and their positional isomers were efficiently prepared by heating 6-bromocycloheptabenzoxazines and the substituted o-aminophenols at 120 deg C in acetic acid.

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