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2-(4-Bromomethyl-phenyl)-naphtho[1,2-d]oxazole is a complex organic chemical compound characterized by a naphtho[1,2-d]oxazole core, which is a fused ring system consisting of a naphthalene and an oxazole. The compound features a bromine atom attached to a methyl group, which is in turn connected to a phenyl ring. This phenyl ring is linked to the naphtho[1,2-d]oxazole system at the 2-position. The presence of the bromine atom makes 2-(4-Bromomethyl-phenyl)-naphtho[1,2-d]oxazole potentially useful in organic synthesis, particularly in reactions where bromine can be replaced by other functional groups, such as in cross-coupling reactions. The compound's structure and reactivity make it a candidate for the development of pharmaceuticals, agrochemicals, or other specialty chemicals where the naphtho[1,2-d]oxazole framework provides a rigid and planar system that can interact with biological targets.

78659-74-2

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78659-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78659-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,5 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78659-74:
(7*7)+(6*8)+(5*6)+(4*5)+(3*9)+(2*7)+(1*4)=192
192 % 10 = 2
So 78659-74-2 is a valid CAS Registry Number.

78659-74-2Downstream Products

78659-74-2Relevant academic research and scientific papers

Synthesis and spectral-luminescence properties of 4,4′-di(2-oxazolyl)-stilbenes and 4,4′-di(2-oxazolyl)tolans

Vernigor,Shalaev,Luk'yanets

, p. 328 - 332 (2007/10/02)

A new method is proposed for the synthesis of 4,4′-di(2-oxazolyl)stilbenes and 4,4′-di(2-oxazolyl) tolans by condensation of oxazolyl-substituted benzyl bromides or benzal dibromides under the influence of strong bases (KOH, potassium tertbutoxide) in dipolar aprotic solvents [dimethylformamide (DMF) and dimethyl sulfoxide (DMSO)]. The synthesized compounds luminesce intensely over the spectral range 386-492 nm.

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