2-Bromo-5-fluoroaniline CAS 1003-99-2

Introduction:Basic information about 2-Bromo-5-fluoroaniline CAS 1003-99-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2-Bromo-5-fluoroaniline Basic information

Product Name:2-Bromo-5-fluoroaniline
Synonyms:2-BROMO-5-FLUOROBENZENAMINE;2-BROMO-5-FLUOROANILINE;2-Bromo-5-fluoro-phenylamine;2-Bromo-5-fluoroaniline 98%;2-Bromo-5-fluoroaniline98%;2-Bromo-5-fluoroaniline,99%;2-Bromo-5-fluoroanil;BenzenaMine, 2-broMo-5-fluoro-
CAS:1003-99-2
MF:C6H5BrFN
MW:190.01
EINECS:
Product Categories:amine| alkyl bromide|alkyl Fluorine;Aryl Fluorinated Building Blocks;Building Blocks;Chemical Synthesis;Fluorinated Building Blocks;Nitrogen Compounds;Organic Building Blocks;Organic Fluorinated Building Blocks;Other Fluorinated Organic Building Blocks;Amines;C2 to C6;Nitrogen Compounds;Aniline;Anilines, Amides & Amines;Bromine Compounds;Fluorine Compounds;Pharmaceutical intermediate;bc0001;C6
Mol File:1003-99-2.mol

2-Bromo-5-fluoroaniline Chemical Properties

Melting point 43-47 °C (lit.)
Boiling point 154 °C / 23mmHg
density 1.694±0.06 g/cm3(Predicted)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka1.52±0.10(Predicted)
form powder to crystal
color White to Light yellow to Dark green
InChIInChI=1S/C6H5BrFN/c7-5-2-1-4(8)3-6(5)9/h1-3H,9H2
InChIKeyFWTXFEKVHSFTDQ-UHFFFAOYSA-N
SMILESC1(N)=CC(F)=CC=C1Br
CAS DataBase Reference1003-99-2(CAS DataBase Reference)

Safety Information

Hazard Codes Xi,T
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR UN2811
WGK Germany 3
Hazard Note Toxic
HazardClass 6.1
PackingGroup III
HS Code 29214200
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3

2-Bromo-5-fluoroaniline Usage And Synthesis

Description2-bromo-5-fluoroaniline: a intermediate of antitumor drug.
2-bromo-5-fluoroaniline is the intermediate of antitumor drug Phortress, phortress is the benzothiazoles CYP1A1 antitumor drugs targeting by Univ Nottingham UK invention, solution becomes lipophilic compound 5F2O3(10 in the sensitive cells but Phortress enters), the latter is as potential aromatic hydrocarbon receptor (AhR) agonist, induce CYP1A1 to express, CYP1A1 metabolism through expressing produces and has high electrophilic active substance again, finally causes DNA damage and apoptosis. The method that, at present, synthetic 2-bromo-5-fluoronitrobenzene prepares 2-bromo-5-fluoroaniline is divided into two large classes:
The one: adopt a chemical reduction method, utilizing the chemical reducing agent reductase 2-bromo-5-fluoronitrobenzenes such as protochloride glass putty, iron powder, vat powder, hydrazine, and sodium borohydride (potassium), which is 2-bromo-5-fluoroaniline.
The 2nd: adopt hydro-reduction. What we do more often both at home and abroad at present is chloride or the catalytic hydrogenation of fluorine-containing arylamine, and the brominated less report of arylamine hydrogenation mainly is easily by hydrogenolysis because of bromine.
Chemical PropertiesYellow to brown crystalline powder
Uses2-Bromo-5-fluoroaniline may be used to synthesize:
  • orthobromothiobenzanilide of 5-fluoronitrobenzothiazole
  • 2-bromo-5-fluorobenzo[14C]nitrile
  • [3-14C]-5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole
  • 2-bromo-5-fluoro-phenyl)-(2-methoxy-6-pentadecyl-benzyl)amine
SynthesisA preparation method of 2-Bromo-5-fluoroaniline is as follows: methanol, 2-bromo-5-fluoronitrobenzene, W-4 type Raney nickel and bromine inhibitor are put into a hydrogenation kettle to carry out hydrogenation reaction. After the reaction is completed, the reaction solution is filtered under nitrogen protection. The filtered filtrate is then distilled under reduced pressure to remove methanol, and n-hexane is added. Then, the product is washed with process water, and after washing, the product is allowed to stand and separate. Then, the organic phase is cooled and crystallized, an off-white to brownish-yellow solid is precipitated, and a wet product is obtained by suction filtration. The wet product is dried to obtain the finished product 2-Bromo-5-fluoroaniline.
References[1] Patent: US2007/259850, 2007, A1. Location in patent: Page/Page column 95-96
[2] Angewandte Chemie - International Edition, 2011, vol. 50, # 51, p. 12257 - 12261
[3] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 23, p. 5259 - 5272
[4] Patent: US2006/94707, 2006, A1. Location in patent: Page/Page column 61
[5] European Journal of Organic Chemistry, 2018, vol. 2018, # 2, p. 209 - 214

2-Bromo-5-fluoroaniline Preparation Products And Raw materials

Raw materials1-BROMO-4-FLUORO-2-NITROBENZENE-->4-Fluoro-2-nitrobenzeneamine-->3-Fluoro-4-broMoaniline-->3-Fluoroaniline-->4-Fluoroacetanilide-->4-Fluoroaniline-->Iron-->4-Bromofluorobenzene-->Sodium hydroxide-->Water
Preparation ProductsNSC-703786-->8-bromo-5-fluoroquinoline-->Pimavanserin
2-Bromo-5-chlorobenzotrifluoride CAS 344-65-0
2-Bromo-5-fluoroanisole CAS 450-88-4
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