5-Bromo-2-(trifluoromethoxy)aniline

Basic Information

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CAS Number

886762-08-9

Molecular Formula

C7H5BrF3NO

Molecular Weight

256.02 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Ethers

Basic Chemical Raw Materials Organic Chemicals Amines

Fine Chemicals Specialty Chemicals UV Stabilizers

Agricultural Chemicals Pesticides Herbicides

Basic Physical Properties

Boiling Point

230.2℃ at 760 mmHg

Density

1.67

SMILES

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C1=CC(=C(C=C1Br)N)OC(F)(F)F

InChI

InChI=1S/C7H5BrF3NO/c8-4-1-2-6(5(12)3-4)13-7(9,10)11/h1-3H,12H2

InChIKey

FOJWHUFRHXEUBA-UHFFFAOYSA-N

LogP

2.9299

Topological Polar Surface Area

35.25 Å²

Hydrogen Bond Donor/Acceptor

2 / 2

Complexity

176

Synonyms & References

English

5-Bromo-2-(trifluoromethoxy)aniline
3-Amino-4-(trifluoromethoxy)bromobenzene
5-bromo-2-(trifluoromethoxy)aniline
5-Bromo-2-(trifluoromethoxy)benzenamine (ACI)
(5-Bromo-2-trifluoromethoxyphenyl)amine
5-Bromo-2-trifluoromethoxyaniline
EN300-247294
5-bromanyl-2-(trifluoromethyloxy)aniline
5-bromo-2-trifluoromethoxyaniline
2-trifluoromethoxy-5-bromo-phenylamine
3-Amino-4-(trifluoromethoxy)BromoBenzene
SY020762
SCHEMBL526369
5-Bromo-2-trifluoromethoxy-phenylamine
CS-W003143
TD1079
DB-024278
2-Amino-4-bromo-trfluoromethoxybenzene
PS-7409
5-bromo-2-trifluoromethoxy aniline
AKOS015834783
DTXSID90381416
886762-08-9
AC-28691
MFCD04039242
A842833

MDL Number

MFCD04039242

Customs Code

2922299090

FAQ

What are the physical and chemical properties of 5-Bromo-2-(trifluoromethoxy)aniline (CAS: 886762-08-9)?

5-Bromo-2-(trifluoromethoxy)aniline is a crystalline solid with a molecular weight of approximately 297.02 g/mol. It is poorly soluble in water but soluble in organic solvents such as methanol and dichloromethane. Chemically, it is relatively stable but can react with reducing agents. It has a strong absorption in the UV-visible region, making it useful for spectroscopic studies.

How is 5-Bromo-2-(trifluoromethoxy)aniline (CAS: 886762-08-9) typically synthesized?

5-Bromo-2-(trifluoromethoxy)aniline is commonly synthesized via bromination of 2-(trifluoromethoxy)aniline. This process typically involves the use of bromine in the presence of a Lewis acid catalyst such as aluminum bromide. The reaction is performed under anhydrous conditions to ensure product purity and high yield.

What industries use 5-Bromo-2-(trifluoromethoxy)aniline (CAS: 886762-08-9)?

5-Bromo-2-(trifluoromethoxy)aniline is used in various industries, including pharmaceuticals, where it serves as a precursor for drug intermediates. It is also utilized in the synthesis of polymers and in sensor technologies due to its unique electronic properties.

What precautions should be taken when handling 5-Bromo-2-(trifluoromethoxy)aniline (CAS: 886762-08-9)?

When handling 5-Bromo-2-(trifluoromethoxy)aniline, it is essential to wear appropriate personal protective equipment (PPE) such as gloves, safety goggles, and a lab coat. Work should be conducted in a well-ventilated area or under a fume hood. Spills should be cleaned up immediately, and proper disposal procedures should be followed. Always refer to the safety data sheet (SDS) for detailed safety information.