NSC10978

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Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:1,2-Dibromo-4-Nitrobenzene
CAS:5411-50-7
Company Name: Career Henan Chemica Co
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Products Intro: Product Name:1,2-DIBROMO-4-NITROBENZENE
CAS:5411-50-7
Purity:98.8%min emma@coreychem.com Package:1KG;2.18USD
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
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CAS:5411-50-7
Company Name: Aromsyn Co., Ltd.
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Products Intro: Product Name:1,2-Dibromo-4-nitrobenzene
CAS:5411-50-7
Purity:NLT 98% Package:1G;1KG;100KG Remarks:AS10433
Company Name: Aceschem Inc.
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Products Intro: Product Name:1,2-Dibromo-4-nitrobenzene
CAS:5411-50-7
Purity:NLT 98% Package:1G;100G;1KG;50KG;100KG Remarks:ACS466570
NSC10978 Basic information
Product Name:NSC10978
Synonyms:NSC10978;1,2-dibroMo-4-nitrobenzen;2-DIBROMO-4-NITROBENZENE;Benzene, 1,2-dibromo-4-nitro-;3,4-Dibromo-1-nitrobenzene
CAS:5411-50-7
MF:C6H3Br2NO2
MW:280.9
EINECS:
Product Categories:
Mol File:5411-50-7.mol
NSC10978 Structure
NSC10978 Chemical Properties
Melting point 58.5°C
Boiling point 296°C (rough estimate)
density 2.2414 (rough estimate)
refractive index 1.6400 (estimate)
storage temp. Sealed in dry,Room Temperature
form solid
color White
Safety Information
HS Code 2904990090
MSDS Information
NSC10978 Usage And Synthesis
Chemical PropertiesYellow needle-like or flaky crystals. Melting point 58-59°C, boiling point 296°C, 180°C (2.66kPa), relative density 2.354 (8/4°C), refractive index 1.9853 (111°C). Soluble in ethanol, benzene and acetic acid, insoluble in water. Can sublimate and volatilize with water vapor.
Synthesis
4-Nitrophthalic acid

610-27-5

NSC10978

5411-50-7

The general procedure for the synthesis of 1,2-dibromo-4-nitrobenzene from 4-nitrophthalic acid was as follows: 4-nitrophthalic acid (1 mmol), bromoisocyanuric acid ester, additives, and solvent (10 ml) were added to a round-bottom flask equipped with a Dimroth condenser (cooled to 10°C). The reaction mixture was heated under magnetic stirring in an oil bath at 120 °C for 60 h under fluorescent room light irradiation (FL). Upon completion of the reaction, the cooled mixture was filtered through a short silica gel pad, washed with 1 M aqueous Na2SO3 solution, dried over Na2SO4, filtered and concentrated in vacuum to give the crude product 1,2-dibromo-4-nitrobenzene. The crude product can be further purified by silica gel chromatography. The experimental results are detailed in Table 6.

References[1] Patent: WO2017/60905, 2017, A1. Location in patent: Paragraph 00164
NSC10978 Preparation Products And Raw materials
Raw materials1-Bromo-4-nitrobenzene-->4-Nitrophthalic acid
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