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4-Bromo-3-nitroanisole

CAS No.
5344-78-5
Chemical Name:
4-Bromo-3-nitroanisole
Synonyms
TIMTEC-BB SBB009974;4-Brom-3-nitroanisol;4-Bromo-3-nitroanisol;4-BROMO-3-NITROANISOLE;4-Bromo-3-nitroanlsole;4-BROMO-3-NITROTHIOANISOLE;4-Bromo-3-nitroanisole >4-bromo-3-nitrobenzyl ether;3-nitro-4-bromobenzyl ether;4-Methoxy-2-nitrobromobenzene
CBNumber:
CB8211332
Molecular Formula:
C7H6BrNO3
Molecular Weight:
232.03
MDL Number:
MFCD00051511
MOL File:
5344-78-5.mol
MSDS File:
SDS
Last updated:2025-08-25 18:08:31
Product description Number Pack Size Price
4-Bromo-3-nitroanisole 97% 338737 5g $31
4-Bromo-3-nitroanisole >96.0%(GC) B3420 5g $39
4-Bromo-3-nitroanisole >96.0%(GC) B3420 25g $127
4-Bromo-3-nitroanisole B688138 5g $75
1-Bromo-4-methoxy-2-nitrobenzene CS-W008002 25g $30
More product size

4-Bromo-3-nitroanisole Properties

Melting point 32-34 °C (lit.)
Boiling point 153-154 °C/13 mmHg (lit.)
Density 1.8134 (rough estimate)
refractive index 1.6090 (estimate)
Flash point >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form powder to lump to clear liquid
color White or Colorles to Yellow to Orange
BRN 2446617
InChI InChI=1S/C7H6BrNO3/c1-12-5-2-3-6(8)7(4-5)9(10)11/h2-4H,1H3
InChIKey KCOBIBRGPCFIGF-UHFFFAOYSA-N
SMILES C1(Br)=CC=C(OC)C=C1[N+]([O-])=O
CAS DataBase Reference 5344-78-5(CAS DataBase Reference)
NIST Chemistry Reference 4-Bromo-3-nitroanisole(5344-78-5)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-24/25
WGK Germany  3
HS Code  29093090
NFPA 704
1
2 0

4-Bromo-3-nitroanisole price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 338737 4-Bromo-3-nitroanisole 97% 5344-78-5 5g $31 2025-07-31 Buy
TCI Chemical B3420 4-Bromo-3-nitroanisole >96.0%(GC) 5344-78-5 5g $39 2025-07-31 Buy
TCI Chemical B3420 4-Bromo-3-nitroanisole >96.0%(GC) 5344-78-5 25g $127 2025-07-31 Buy
TRC B688138 4-Bromo-3-nitroanisole 5344-78-5 5g $75 2021-12-16 Buy
ChemScene CS-W008002 1-Bromo-4-methoxy-2-nitrobenzene 5344-78-5 25g $30 2021-12-16 Buy
Product number Packaging Price Buy
338737 5g $31 Buy
B3420 5g $39 Buy
B3420 25g $127 Buy
B688138 5g $75 Buy
CS-W008002 25g $30 Buy

4-Bromo-3-nitroanisole Chemical Properties,Uses,Production

Chemical Properties

Yellow to dark brown solid

Uses

4-Bromo-3-nitroanisole was used in the synthesis of:

  • 4-bromo-5-methoxyaniline
  • 2-(4-methoxy-2-nitrophenylsulfanyl)benzoic acid
  • 4-(1-diethylamino-4-pentylamino)-3-nitrochlorobenzene

General Description

FT-IR and FT-Raman spectra of 4-bromo-3-nitroanisole have been studied.

Synthesis

Azoic Diazo Component 1

96-96-8

4-Bromo-3-nitroanisole

5344-78-5

The general procedure for the synthesis of 4-bromo-3-nitroanisole from ice-dyed diazo component 1 was as follows: a solution of sodium nitrite (11.8 g) in water (28 mL) was slowly added dropwise to a 40% solution of nitroaniline (125 mmol) in hydrobromic acid (110 g) over a period of 0.5 h. The temperature of the reaction was maintained at 10 °C. The reaction mixture was stirred at 0-10 °C for 40 min and then filtered. Subsequently, the filtrate was added dropwise to a purple solution of copper(I) bromide (209 mmol) in hydrobromic acid (74 mL) at 0 °C over a period of 1 hour. The reaction mixture was gradually warmed to room temperature and held for 30 min, then warmed to 60 °C for 0.5 h. The reaction was finally heated and refluxed for 1 h. The reaction was carried out at a temperature of 0.5 °F to 0.5 °F. After completion of the reaction, the mixture was partitioned between water (2.0 L) and dichloromethane (600 mL) and the aqueous phase was then extracted with dichloromethane (300 mL). All organic layers were combined and washed sequentially with 10% sodium hydroxide solution (200 mL), water (600 mL), 10% hydrochloric acid (300 mL) and water (600 mL). The organic layer was dried over magnesium sulfate and concentrated to give 4-bromo-3-nitroanisole in 83% yield as a yellow oil.

References

[1] Journal of Organic Chemistry, 1989, vol. 54, # 25, p. 5856 - 5866
[2] Journal of Organic Chemistry, 1992, vol. 57, # 24, p. 6380 - 6382
[3] Journal of the American Chemical Society, 1994, vol. 116, # 26, p. 11797 - 11810
[4] Tetrahedron Letters, 2006, vol. 47, # 16, p. 2739 - 2742
[5] Tetrahedron, 2010, vol. 66, # 37, p. 7418 - 7422

33844-21-2
5344-78-5
Synthesis of 4-Bromo-3-nitroanisole from 4-Methoxy-2-nitrobenzoic acid
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View Lastest Price from 4-Bromo-3-nitroanisole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4-Bromo-3-nitroanisole pictures 2025-12-17 4-Bromo-3-nitroanisole
5344-78-5
US $0.00 / KG 25KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
4-Bromo-3-nitroanisole pictures 2025-11-19 4-Bromo-3-nitroanisole
5344-78-5
US $0.00 / kg 1kg 99.0% 1000kg Shanghai Joiny Pharmaceutical Co.,LTD
4-Bromo-3-Nitroanisole pictures 2025-08-26 4-Bromo-3-Nitroanisole
5344-78-5
US $0.00-0.00 / kg 1kg 99% 1 Jinan Ruitong Biotech Co., Ltd.
1-Bromo-4-methoxy-2-nitrobenzene 4-Bromo-3-nitroanisol Benzene, 1-bromo-4-methoxy-2-nitro- 4-BROMO-3-NITROTHIOANISOLE 4-BROMO-3-NITROANISOLE TIMTEC-BB SBB009974 4-bromo-3-nitrobenzyl ether 4-Methoxy-2-nitrobromobenzene 1-Bromo-2-nitro-4-methoxybenzene 1-Nitro-2-bromo-5-methoxybenzene 4-Methoxy-2-nitrophenyl bromide 1-((4-((E)-2-nitrovinyl)phenoxy)methyl)benzene 4-Bromo-3-nitroanlsole 4-Bromo-3-nitroanisole > 4-Brom-3-nitroanisol 3-nitro-4-bromobenzyl ether 5344-78-5 Organic Building Blocks Nitrogen Compounds Nitro Compounds Building Blocks ARYL HALIDE Phenyls & Phenyl-Het Nitro Compounds Nitrogen Compounds Organic Building Blocks blocks Bromides NitroCompounds Halides Phenyls & Phenyl-Het Anisole Anisoles, Alkyloxy Compounds & Phenylacetates Bromine Compounds Nitro Compounds