4-NITRO N-BUTYL ANILINE

4-NITRO N-BUTYL ANILINE Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:58259-34-0
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
Company Name: Accela ChemBio Inc.
Tel: +1-858-6993322 +86-18019713315
Email: info@accelachem.com
Products Intro: Product Name:N-Butyl-4-nitroaniline
CAS:58259-34-0
Purity:>=97% Package:0.1g;0.25g;1g;5g
Company Name: Fuxin Pharmaceutical
Tel: +86-021-021-50872116
Email: contact@fuxinpharm.com
Products Intro: Product Name:N-Butyl-4-nitroaniline
CAS:58259-34-0
Purity:0.98 Package:1kg; 25kg; or larger package as required Remarks:pharmaceutical intermediates;Chemical Intermediate
Company Name: Aromsyn Co., Ltd.
Tel: +86-0571-85585865 +86-13336024896
Email: CB@aromsyn.com
Products Intro: Product Name:4-Nitron-butylaniline
CAS:58259-34-0
Purity:NLT 95% Package:1G;1KG;100KG Remarks:AS93438
Company Name: Sichuan Biosynce Pharmatech Co., Ltd.
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Email: diane@biosynce.com
Products Intro: Product Name:N-Butyl-4-nitroaniline
CAS:58259-34-0
Purity:0.95_) Package:100G;500G;1KG Remarks:Chemically Pure
4-NITRO N-BUTYL ANILINE Basic information
Product Name:4-NITRO N-BUTYL ANILINE
Synonyms:4-NITRO N-BUTYL ANILINE;N-Butyl-4-nitroaniline;1-[Butylamino]-4-nitrobenzene;N-Butyl-4-nitrobenzenamine;Benzenamine, N-butyl-4-nitro-
CAS:58259-34-0
MF:C10H14N2O2
MW:194.23
EINECS:
Product Categories:
Mol File:58259-34-0.mol
4-NITRO N-BUTYL ANILINE Structure
4-NITRO N-BUTYL ANILINE Chemical Properties
storage temp. Keep in dark place,Inert atmosphere,Room temperature
Safety Information
HS Code 2921490090
MSDS Information
4-NITRO N-BUTYL ANILINE Usage And Synthesis
Synthesis
4-Nitrophenol

100-02-7

Butylamine

109-73-9

4-NITRO N-BUTYL ANILINE

58259-34-0

Using 4-nitrophenol (209 mg, 1.5 mmol) and n-butylamine (2.9 mL, 30 mmol), 4-nitrophenol was dissolved in N,N-dimethylformamide (2 mL) under nitrogen protection, n-butylamine was added, and the reaction was carried out for 9 hours at 120 °C. After completion of the reaction, it was cooled to room temperature and the reaction mixture was poured into water (16 mL) and extracted with dichloromethane (3 x 5 mL). The organic phases were combined, washed with saturated saline (2 × 4 mL), dried over anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel column chromatography with the eluent of dichloromethane:methanol (100:1, v/v) gave the target product N-butyl-4-nitroaniline as a yellow liquid in 64% yield.

References[1] Patent: CN106631820, 2017, A. Location in patent: Paragraph 0035; 0036; 0037; 0038
4-NITRO N-BUTYL ANILINE Preparation Products And Raw materials
Raw materialsN-(4-nitrophenyl)butanamide-->4-Nitrophenol-->Butylamine-->1-Iodo-4-nitrobenzene-->1-Bromo-4-nitrobenzene
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