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ChemicalBook >> CAS DataBase List >>2-BroMo-1,3-diMethyl-4-nitrobenzene

2-BroMo-1,3-diMethyl-4-nitrobenzene

CAS No.
60956-25-4
Chemical Name:
2-BroMo-1,3-diMethyl-4-nitrobenzene
Synonyms
2,6-Dimethyl-3-nitrobromobenzene;1,3-Dimethyl-2-bromo-4-nitrobenzene;2-BroMo-1,3-diMethyl-4-nitrobenzene;Benzene, 2-bromo-1,3-dimethyl-4-nitro-
CBNumber:
CB02662778
Molecular Formula:
C8H8BrNO2
Molecular Weight:
230.06
MDL Number:
MFCD11878621
MOL File:
60956-25-4.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:51

2-BroMo-1,3-diMethyl-4-nitrobenzene Properties

Melting point 53 °C(Solv: ethanol (64-17-5))
Boiling point 290.7±35.0 °C(Predicted)
Density 1.533±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Appearance Off-white to light yellow Solid

2-BroMo-1,3-diMethyl-4-nitrobenzene price More Price(16)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B700655 2-Bromo-1,3-dimethyl-4-nitrobenzene 60956-25-4 500mg $130 2021-12-16 Buy
ChemScene CS-0139918 2-Bromo-1,3-dimethyl-4-nitrobenzene 60956-25-4 5g $252 2021-12-16 Buy
ChemScene CS-0139918 2-Bromo-1,3-dimethyl-4-nitrobenzene 60956-25-4 1g $76 2021-12-16 Buy
AK Scientific 9113AB 2-Bromo-1,3-dimethyl-4-nitrobenzene 60956-25-4 1g $112 2021-12-16 Buy
American Custom Chemicals Corporation HCH0363087 2-BROMO-1,3-DIMETHYL-4-NITROBENZENE 95.00% 60956-25-4 5MG $505.93 2021-12-16 Buy
Product number Packaging Price Buy
B700655 500mg $130 Buy
CS-0139918 5g $252 Buy
CS-0139918 1g $76 Buy
9113AB 1g $112 Buy
HCH0363087 5MG $505.93 Buy

2-BroMo-1,3-diMethyl-4-nitrobenzene Chemical Properties,Uses,Production

Synthesis

2-Bromo-m-xylene

576-22-7

2-BroMo-1,3-diMethyl-4-nitrobenzene

60956-25-4

General procedure for the synthesis of 2-bromo-1,3-dimethyl-4-nitrobenzene from 2,6-dimethylbromobenzene: Step 1: At -10°C, 2-bromo-1,3-dimethylbenzene (5.0 g, 27.03 mmol) was dissolved in 98% sulfuric acid (40 mL), and a mixed solution consisting of 68% nitric acid (2.74 g, 27.03 mmol) and 98% sulfuric acid (10 mL) was slowly added dropwise. After the reaction was completed, the mixture was continued to be stirred at -10°C for 1 hour. Subsequently, the reaction mixture was quenched by pouring it into ice (200 g), the precipitated solid was collected by filtration, washed with water and dried under vacuum. The crude product was purified by silica gel column chromatography using petroleum ether/ethyl acetate (100:1) as eluent to afford 2.3 g (37% yield) of 2-bromo-1,3-dimethyl-4-nitrobenzene as a yellow solid. The structure of the product was confirmed by 1H NMR (500 MHz, DMSO-d6): δ 7.79 (d, J=8.5 Hz, 1H), 7.43 (d, J=8.5 Hz, 1H), 2.47 (s, 3H), 2.44 (s, 3H).

References

[1] Patent: WO2013/26914, 2013, A1. Location in patent: Page/Page column 170
[2] Tetrahedron, 1977, vol. 33, p. 2965 - 2967
[3] Patent: WO2004/43925, 2004, A2. Location in patent: Page 68
[4] Patent: WO2007/21937, 2007, A2. Location in patent: Page/Page column 42
[5] Patent: WO2008/79918, 2008, A1. Location in patent: Page/Page column 61

2-BroMo-1,3-diMethyl-4-nitrobenzene Preparation Products And Raw materials

Raw materials

Preparation Products

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ATK CHEMICAL COMPANY LIMITED
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2-BroMo-1,3-diMethyl-4-nitrobenzene Spectrum

2-BroMo-1,3-diMethyl-4-nitrobenzene 1,3-Dimethyl-2-bromo-4-nitrobenzene Benzene, 2-bromo-1,3-dimethyl-4-nitro- 2,6-Dimethyl-3-nitrobromobenzene 60956-25-4