ChemicalBook > CAS DataBase List > 4-Bromo-3,5-difluoroaniline

4-Bromo-3,5-difluoroaniline

Product Name
4-Bromo-3,5-difluoroaniline
CAS No.
203302-95-8
Chemical Name
4-Bromo-3,5-difluoroaniline
Synonyms
BUTTPARK 35\03-50;4-BROMO-3,5-DIFLUOROANILINE;4-Bromo-3,5-difluoroaniline >4-Bromo-3,5-difluoroaniline 95%;4-bromo-3,5-difluoro-Benzenamine;Benzenamine, 4-bromo-3,5-difluoro-;4-Bromo-3,5-difluoroaniline ISO 9001:2015 REACH;4-BroMo-3,5-difluoroaniline 95%, 5-difluoroaniline 95%
CBNumber
CB8767273
Molecular Formula
C6H4BrF2N
Formula Weight
208
MOL File
203302-95-8.mol
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4-Bromo-3,5-difluoroaniline Property

Melting point:
99-101°C
Boiling point:
223.7±35.0 °C(Predicted)
Density 
1.788±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
1.86±0.10(Predicted)
color 
White to Light gray to Light orange
InChI
InChI=1S/C6H4BrF2N/c7-6-4(8)1-3(10)2-5(6)9/h1-2H,10H2
InChIKey
DKKUSFDAHRASGO-UHFFFAOYSA-N
SMILES
C1(N)=CC(F)=C(Br)C(F)=C1
CAS DataBase Reference
203302-95-8(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
RIDADR 
UN2811
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
III
HS Code 
2921420090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H312Harmful in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H331Toxic if inhaled

H335May cause respiratory irritation

Precautionary statements

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

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

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

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

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

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TCI Chemical
Product number
B3416
Product name
4-Bromo-3,5-difluoroaniline
Purity
>98.0%(GC)(T)
Packaging
5g
Price
$62
Updated
2025/07/31
TCI Chemical
Product number
B3416
Product name
4-Bromo-3,5-difluoroaniline
Purity
>98.0%(GC)(T)
Packaging
25g
Price
$247
Updated
2025/07/31
TRC
Product number
B678980
Product name
4-Bromo-3,5-difluoroaniline
Packaging
5g
Price
$70
Updated
2021/12/16
TRC
Product number
B678980
Product name
4-Bromo-3,5-difluoroaniline
Packaging
100mg
Price
$45
Updated
2021/12/16
SynQuest Laboratories
Product number
3630-B-43
Product name
4-Bromo-3,5-difluoroaniline
Purity
98%
Packaging
25g
Price
$49
Updated
2021/12/16
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4-Bromo-3,5-difluoroaniline Chemical Properties,Usage,Production

Chemical Properties

Pale yellow powder

Uses

4-Bromo-3,5-difluoroaniline is a useful reactant in organic synthesis.

Synthesis

372-39-4

203302-95-8

General procedure for the synthesis of 3,5-difluoro-4-bromoaniline from 3,5-difluoroaniline: 1. 3,5-difluoroaniline (10.0 g, 77.5 mmol) was dissolved in DMF (100 mL), then NBS (13.9 g, 78.0 mmol) was added in batches at room temperature. The reaction mixture was stirred overnight at room temperature and then diluted with Et2O and washed with brine. The organic phase was separated, dried over Na2SO4 and concentrated to give an oil. Purification by column chromatography afforded 4-bromo-3,5-difluoroaniline (i) (12.9 g, 80.2%). 2. A mixture of 4-bromo-3,5-difluoroaniline(i) (6.0 g, 28.8 mmol), ferrous sulfate (1.82 g), glycerol (8.6 mL), nitrobenzene (1.79 mL) and concentrated sulfuric acid (5.0 mL) was gently heated. After the first vigorous reaction, the mixture was boiled for 5 hours. Nitrobenzene was removed by vacuum distillation and the aqueous solution was acidified with glacial acetic acid to isolate a dark brown precipitate. Purification by rapid chromatography (silica gel, petroleum ether/ethyl acetate = 12/1) gave 6-bromo-5,7-difluoroquinoline (ii) as a white solid (3.5 g, 49.8%). 3. To a solution of 6-bromo-5,7-difluoroquinoline(ii) (250 g, 1.02 mol) in anhydrous THF (2200 mL) was added dropwise a hexane solution of n-BuLi (2.5 M, 408 mL, 1.02 mol) at -78 °C. The resulting mixture was stirred at -78 °C for another 30 min. Then, anhydrous THF (200 mL) solution of DMF (79 mL, 1.02 mol) was added while the temperature was kept below -70 °C and the mixture was stirred at the same temperature for 30 min. The reaction mixture was slowly warmed to room temperature and diluted with saturated aqueous NH4Cl solution (1000 mL) and water (800 mL). The mixture was extracted twice with ethyl acetate and the combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate and concentrated to give a brown oil. Purification by silica gel column chromatography, eluting with petroleum ether and ethyl acetate (10:1), afforded 5,7-difluoroquinoline-6-carbaldehyde (Intermediate H) as a yellow solid (100 g, 50%). 1H NMR (DMSO, 300 MHz) δ (ppm): 10.38 (s, 1H), 9.10~9.12 (m, 1H), 8.62~8.66 (m, 1H), 7.68~7.78 (m, 2H).

References

[1] Patent: WO2011/18454, 2011, A1. Location in patent: Page/Page column 59-60
[2] Patent: WO2004/48314, 2004, A1. Location in patent: Page 31-32
[3] Patent: US2017/137385, 2017, A1. Location in patent: Paragraph 0243; 0244; 0245; 0246

4-Bromo-3,5-difluoroaniline Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 4-Bromo-3,5-difluoroaniline manufacturers

Career Henan Chemical Co
Product
4-Bromo-3,5-difluoroaniline 203302-95-8
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100kg
Release date
2019-07-11