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2-Bromo-4-nitrobenzaldehyde

Uses
Product Name
2-Bromo-4-nitrobenzaldehyde
CAS No.
5274-71-5
Chemical Name
2-Bromo-4-nitrobenzaldehyde
Synonyms
2-Bromo-4-nitrobenzaldehyde;Benzaldehyde, 2-broMo-4-nitro-;ethyl 6-amino-4-(4-bromothiophen-2-yl)-5-cyano-2-propyl-4H-pyran-3-carboxylate
CBNumber
CB91509107
Molecular Formula
C7H4BrNO3
Formula Weight
230.02
MOL File
5274-71-5.mol
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2-Bromo-4-nitrobenzaldehyde Property

Melting point:
81-82 °C
Boiling point:
334.3±27.0 °C(Predicted)
Density 
1.781±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
Pale yellow
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Safety

HS Code 
2913000090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
B704453
Product name
2-Bromo-4-nitrobenzaldehyde
Packaging
50mg
Price
$45
Updated
2021/12/16
TRC
Product number
B704453
Product name
2-Bromo-4-nitrobenzaldehyde
Packaging
500mg
Price
$265
Updated
2021/12/16
ChemScene
Product number
CS-W003568
Product name
2-Bromo-4-nitrobenzaldehyde
Packaging
250mg
Price
$35
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB32155
Product name
2-Bromo-4-nitrobenzaldehyde
Packaging
50mg
Price
$60
Updated
2021/12/16
SynQuest Laboratories
Product number
4654-9-15
Product name
2-Bromo-4-nitrobenzaldehyde
Packaging
250mg
Price
$61
Updated
2021/12/16
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2-Bromo-4-nitrobenzaldehyde Chemical Properties,Usage,Production

Uses

2-Bromo-4-nitrobenzaldehyde can be used as a pharmaceutical synthesis intermediate.

Synthesis

7745-93-9

5274-71-5

GENERAL STEPS: 2-Bromo-1-methyl-4-nitrobenzene (15.0 g, 69.4 mmol) was dissolved in a mixture of peracetic acid (112 mL) and acetic anhydride (105 mL, 1,113 mmol). The reaction mixture was cooled in an ice water bath and concentrated sulfuric acid (15 mL, 281 mmol) was added slowly. Subsequently, chromium (VI) oxide (34.7 g, 347 mmol) was added in batches while the reaction temperature was strictly controlled in the range of 5-10 °C. The reaction mixture was continuously stirred in an ice bath for 1.5 h, during which the temperature needed to be closely monitored, and an ice-acetone bath was used to maintain the temperature at no more than 10 °C if necessary. Upon completion of the reaction, the mixture was poured into a 2 L conical flask containing an appropriate amount of ice, and the total volume was adjusted to 1,500 mL by adding cold water.The precipitate was collected through a Brinell funnel and washed with cold water until nearly colorless. The resulting solid was suspended in cold 2% aqueous Na2CO3 solution (100 mL), stirred thoroughly and the solid was again collected, washed with cold water and partially dried over a Brinell's funnel to give 8.3 g of crude diacetate intermediate. The intermediate (8.3 g) was mixed with ethanol (16 mL), water (16 mL) and concentrated sulfuric acid (2.4 mL) and heated to reflux for 1 hour. After cooling to room temperature, the mixture was transferred to a split funnel containing saturated aqueous K2CO3 solution (50 mL). Fluffy solid formation was observed and identified as non-target product. The aqueous layer was extracted with ethyl acetate (4 x 50 mL), the organic layers were combined and washed with brine (25 mL), dried over MgSO4, filtered and concentrated. Purification by silica gel column chromatography (gradient elution of 5%-15% ethyl acetate in hexane solution) afforded 2-bromo-4-nitrobenzaldehyde (1.41 g, 9% yield) as a colorless fluffy solid.1H NMR (400 MHz, CDCl3) δ 10.41 (s, 1H), 8.51 (d, J = 2.0 Hz, 1H), 8.25 (dd, J = 8.4), 2.1 Hz, 2.1 Hz, 1 Hz. , 2.1 Hz, 1H), 8.06 (d, J = 8.6 Hz, 1H).

References

[1] Patent: WO2015/6100, 2015, A1. Location in patent: Page/Page column 75; 76
[2] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 12, p. 2059 - 2063
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 9, p. 1323 - 1326
[4] Chemical Communications, 2011, vol. 47, # 23, p. 6635 - 6637
[5] European Journal of Organic Chemistry, 2011, # 28, p. 5626 - 5635

2-Bromo-4-nitrobenzaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Bromo-4-nitrobenzaldehyde Suppliers

Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
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sales@accelachem.com
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China
ProdList
11035
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64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
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64
Beijing Eternalchem Co,. Ltd.
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010-59484199 18611897322
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sales@eternalchem.com
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China
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Hangzhou Sage Chemical Co., Ltd.
Tel
+86057186818502 13588463833
Fax
Pls mail us for more information!
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Country
China
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Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
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SHANGHAI FORTUNE CHEMICAL TECHNOLOGY CO., LTD
Tel
13816107857
Fax
qq: 276312098
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sales@fortunechem-sh.com
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CEG Chemical Science&Technology Co., Ltd.
Tel
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Bide Pharmatech Ltd.
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400-164-7117 13681763483
Fax
+86-21-61629029
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Nantong MYBio-pharm. Co., Ltd.
Tel
0513-85921823 18662920231
Fax
86-513-85012876
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Shanghai ChuangYan Chemical Technology Co., Ltd.
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021-11111111 11111111111
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qq:546919421
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View Lastest Price from 2-Bromo-4-nitrobenzaldehyde manufacturers

R&D Scientific Inc.
Product
2-Bromo-4-nitrobenzaldehyde 5274-71-5
Price
US $1120.00/g
Min. Order
1g
Purity
98
Supply Ability
500 Kg
Release date
2024-03-20
Career Henan Chemical Co
Product
2-Bromo-4-nitrobenzaldehyde 5274-71-5
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100KG
Release date
2019-12-25