4-(2-nitro phenylthio)benzaldehyde

Base Information

Chemical Name:4-(2-nitro phenylthio)benzaldehyde
CAS No.:126585-08-8
Molecular Formula:C₁₃H₉NO₃S
Molecular Weight:259.285
Hs Code.:

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-(2-nitro phenylthio)benzaldehyde

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Technology Process of 4-(2-nitro phenylthio)benzaldehyde

There total 3 articles about 4-(2-nitro phenylthio)benzaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 88-73-3
2-Chloronitrobenzene

: 126585-08-8
4-(2-nitro phenylthio)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / sodium ethylate / ethanol / 3 h / Ambient temperature

2: 1.) NBS, benzoyl-peroxide; 2.) silver nitrate / 1.) CCl₄, reflux, 15 h; 2.) acetone, water, room temp., 1 h

With N-Bromosuccinimide; Perbenzoic acid; sodium ethanolate; silver nitrate; In ethanol;

Reference yield:

: 106-45-6
para-thiocresol

: 126585-08-8
4-(2-nitro phenylthio)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / sodium ethylate / ethanol / 3 h / Ambient temperature

2: 1.) NBS, benzoyl-peroxide; 2.) silver nitrate / 1.) CCl₄, reflux, 15 h; 2.) acetone, water, room temp., 1 h

With N-Bromosuccinimide; Perbenzoic acid; sodium ethanolate; silver nitrate; In ethanol;

Reference yield:

: 20912-17-8
2-(4-methylphenylsulfanyl)nitrobenzene

: 126585-08-8
4-(2-nitro phenylthio)benzaldehyde

: 126585-07-7
4-(2-nitro phenylthio)benzoic acid

Guidance literature:: With N-Bromosuccinimide; Perbenzoic acid; silver nitrate; Yield given. Multistep reaction. Yields of byproduct given; 1.) CCl₄, reflux, 15 h; 2.) acetone, water, room temp., 1 h;