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2-(4-nitrophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine is a complex organic chemical compound with the molecular formula C18H13NO3. It is characterized by a naphthalene core, which is fused with a 1,3-oxazine ring. The compound features a 4-nitrophenyl group attached to the 2-position of the naphthalene, and the molecule is in a 2,3-dihydro configuration, indicating the presence of two hydrogen atoms in the molecule's structure. 2-(4-nitrophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine is likely to be used in advanced chemical research or as an intermediate in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and functional groups.

6625-52-1

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6625-52-1 Usage

Chemical structure

2-(4-nitrophenyl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine

Type

Fluorescent dye

Usage

Staining biological materials (e.g. cell membranes, lipid droplets), detection of polymeric materials, analysis of environmental contaminants

Properties

High quantum yield, good photostability

Popularity

Widely used in fluorescence microscopy and other imaging techniques

Potential applications

Development of fluorescent sensors for detection of compounds (e.g. drugs, explosives)

Check Digit Verification of cas no

The CAS Registry Mumber 6625-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6625-52:
(6*6)+(5*6)+(4*2)+(3*5)+(2*5)+(1*2)=101
101 % 10 = 1
So 6625-52-1 is a valid CAS Registry Number.

6625-52-1Downstream Products

6625-52-1Relevant academic research and scientific papers

Ultrasound-assisted one-pot synthesis of 1,3-oxazine derivatives catalysed by BF3-SiO2 under neat conditions

Reddy, Mudumala Veeranarayana,Lim, Kwon Taek,Kim, Jong Tae,Jeong, Yeon Tae

experimental part, p. 398 - 401 (2012/09/21)

An efficient and environment-friendly method for the synthesis of 1,3-oxazine derivatives has been developed using the ultrasound-mediated condensation of 2-naphthol with formaldehyde and primary amines under solvent-free condition at room temperature in

Polyethylene glycol (PEG) mediated expeditious synthetic route to 1,3-oxazine derivatives

Shinde, Pravin V.,Kategaonkar, Amol H.,Shingate, Bapurao B.,Shingare, Murlidhar S.

experimental part, p. 915 - 918 (2012/01/11)

Various 1,3-oxazine derivatives were synthesized in high yields, within shorter reaction times using PEG-400 as a safer medium/mediator. This synthetic route is exceedingly easy and avoids the use of acid/base catalysts.

An efficient one-pot strategies for the synthesis of [1,3] oxazine derivatives

Sapkal, Suryakant B.,Shelke, Kiran F.,Shingate, Bapurao B.,Shingare, Murlidhar S.

experimental part, p. 437 - 442 (2010/10/19)

Sodium hydrogen sulphate (NaHSO4), n-tetra butyl ammonium bromide (TBAB) as a phase transfer catalyst (PTC) in water, and 1-butyl-3-methyl imidazolium hydrogen sulphate [bmim]HSO4 as ionic liquid (IL) has been used as a mild reaction promoter for the cyclocondensation of formalin, β-naphthol and aromatic amines to afford respective 2,3-dihydro-2-phenyl- 1H-naphtho-[1,2-e] [1,3] oxazine derivatives. The present protocols are greener, high yielding and involved the nonchromatographic isolation procedure.

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