914635-64-6

Basic information

• Product Name: 2-BROMO-3-METHOXYBENZOTRIFLUORIDE
• Synonyms: 2-BROMO-3-METHOXYBENZOTRIFLUORIDE;2-Bromo-3-(trifluoromethyl)anisole;2-Bromo-3-(trifluoromethyl)anisole, 2-Bromo-1-methoxy-3-(trifluoromethyl)benzene;2-Bromo-1-methoxy-3-(trifluoromethyl)benzene
• CAS NO: 914635-64-6
• Molecular Formula: C8H6BrF3O
• Molecular Weight: 255.03
• Mol File: 914635-64-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 212.3±40.0 °C(Predicted)
• Appearance: /
• Density: 1.563±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-BROMO-3-METHOXYBENZOTRIFLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-3-METHOXYBENZOTRIFLUORIDE(914635-64-6)
• EPA Substance Registry System: 2-BROMO-3-METHOXYBENZOTRIFLUORIDE(914635-64-6)

Safety Data

• Hazard Codes: T
• Hazardous Substances Data: 914635-64-6(Hazardous Substances Data)

Usage

General Description

2-Bromo-3-methoxybenzotrifluoride is a chemical compound that belongs to the class of benzotrifluorides. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. 2-BROMO-3-METHOXYBENZOTRIFLUORIDE is known for its high reactivity and is commonly used in organic synthesis. It is a colorless liquid with a strong and distinctive odor. 2-Bromo-3-methoxybenzotrifluoride is flammable and should be handled with caution, following appropriate safety measures.

Upstream product

• 386-72-1 2-nitro-3-(trifluoromethyl)phenol 
• 133863-87-3 2-methoxy-6-(trifluoromethyl)aniline 
• 454-90-0 3-(trifluoromethyl)anisole 

Relevant articles and documents

INHIBITING HUMAN INTEGRIN α4β7

Disclosed are small molecule antagonists of human α4β7 integrin, and methods of using them to treat a number of diseases and conditions.

Ring-Substituted y1,2-Bis(4-hydroxyphenyl)ethylenediamine>dichloroplatinum(II) Complexes: Compounds with a Selective Effect on the Hormone-Dependent Mammary Carcinoma

dichloroplatinum(II) complexes with one substituent in the 2-position (CH3, CF3, F, Br, I: meso- and dl-1-PtCl2, meso-(3-5)-PtCl2, meso-(7 and 8)-PtCl2) or two substituents in the 2,6-position (CH3, Cl: meso-2-PtCl2, meso- and dl-6-PtCl2) in both benzene rings were synthesized and tested for estrogenic and toxic activities.Two complexes (meso-6-PtCl2 and meso-7-PtCl2) possess both effects.In comparative tests on estrogen receptor positive and negative mammary tumors in cell culture (MCF 7, ER+ and MDA-MB 231, ER-) and in animals (MXT, ER+ and MXT, ER-, mouse), meso-6-PtCl2 shows a selective effect on the estrogen receptor positive mammary carcinoma.A further increase of efficacy was achieved with the water-soluble (sulfato)platinum(II) derivative (meso-6-PtSO4).On the DMBA-induced hormone dependent mammary carcinoma of the SD rat, meso-6-PtSO4 is significantly more active than its ligand (meso-6) and cisplatin.