- Fluorite Raw Material
- Inorganic Fluorine Products
-
Organic Fluorine Products
- Organic Solvent
- Perfluorinated Vinyl Ethers (PFVEs)
- 2,3,5-Trifluoropyridine
- Bisphenol AF(BPAF)
- Hexafluoroisopropanol
- PFA
- FEP
- PTFE
- Fluorocarbon Solvent
- Hexafluoropropylene Oxide (HFPO)
- Hexafluoropropylene
- Hexafluorobutadiene
- Perfluorohexanoic Acid
- Octafluorocyclobutane C318
- Chlorotrifluoroethylene CTFE
- Nuclear-Grade Boron Material
- Metaphosphate Series
- High-Purity Fluoride Series
- High Purity Rare Gases and Fluorine-Containing Gases
- High-Purity Fluoride Salts
- Perfluoropolyether Product Series
- Lithium Battery Materials
-
Fluorine-Containing Intermediates
- Perfluoropolyether
- 4-Fluorobenzoyl chloride
- Fluorobenzene
- M-Trifluoromethylbenzeneacetonitrile
- 2,4-Dichloro-3,5-Dinitrobenzotrifluoride
- Ethiopromide
- 2-Bromoheptafluoropropane
- 2-Amino-5-Chloro-2'-Fluorobenzophenone
- 2-Fluoro-4-Bromoaniline
- 3,5-Difluorobromobenzene
- 3,4,5-Trifluorobromobenzene
- M-Fluorophenol
- Bromo-3-Fluorobenzene
- Pentafluorobenzyl Bromide
- Ethyl Difluoroacetate
- Ethyl Difluorobromoacetate
- Trifluorochloric Acid
- Fluoropolymers and Fluorine-Containing Materials
- Ultraviolet Absorber
- Pharmaceuticals
-
Customized Product
-
Other Customized Products
- Trifluoromethoxybenzene Series
- Fluorinated Nitrobenzene Series
- Fluorinated Toluene Series
- Fluorinated Benzonitrile Series
- Fluorinated Benzoic Acid Series
- Fluorobenzaldehyde Series
- Fluorinated Anisole Series
- Fluorinated Phenol Series
- 3-difluoromethyl-1-Methyl-1H-Pyrazole-4-Carboxlic Acid
- Methanol
- Boric Acid
- Urea Ammonium Nitrate Solution
- 2-Diazo-1-Naphthol-5-Sulfonyl Chloride
- Propargyl Alcohol
- 1,4-Butynediol
- Zirconium Dioxide
- Lithium Carbonate
- 8-Chlorotheophylline
- Methyl Sulfoxide (DMSO)
- Sodium Hexafluoroantimonate
- Boron-10
- Aprepitant--Adjuvant Anti-Vomiting For Cancer Chemotherapy
- Trifluoro Derivative Series
- Lithium Salt-LiTFSi Series
- Perfluorinated Series
-
Trifluorotoluene Series
- 2,4-Dichloro-3,5-Dinitrotrifluorotoluene
- M-Fluorotrifluorotoluene
- O-Fluorotrifluorotoluene
- P-Fluorotrifluorotoluene
- 2-Bromo-5-Fluorotrifluorotoluene
- 5-Bromo-2-Fluorotrifluorotoluene
- 5-Chloro-2-Nitrotrifluorotoluene
- 4-Fluoro-3-Trifluoromethylphenol
- P-Trifluoromethylthiophenol
- M-Ditrifluorotoluene
- 3.5-Bistrifluoromethylbromobenzene
- P-Ditrifluorotoluene
- 2. 4. 6-Trifluorobenzonitrile
-
Other Customized Products
01
Ethyl bromodifluoroacetate (BDFA)
BRIEF DESCRIPTION
Ethyl difluorobromoacetate compound is an intermediate in the synthesis of drugs and high-energy materials. For example, ethyl difluorobromoacetate is an intermediate for the anti-tumor drug gemcitabine.

TECHNICAL INDICATORS
| Analysis | Requirement |
| Appearance | Colorless Transparent Liquid |
| Purity (% by weight) | 99.29% |
| ≤0.50% | 0.25% |
| ≤0.20% | 0.20% |
| Boiling Point (℃) | 112 °C/700 mmHg (lit.) |
| Density (kg/m) | 1.583 g/mL at 25 °C (lit.) |
| Flash Point (℃) | 70 °F |
USE
1. As an important organic synthesis intermediate, ethyl difluorobromoacetate is widely used in pharmaceuticals, pesticides and other fields.
2. It can be used to synthesize fluorine-containing organic compounds, such as fluoroketones, fluoramides, etc.
STORAGE CONDITIONS
1. During the operation of ethyl difluorobromoacetate, you need to pay attention to protective equipment, including respirators, protective glasses and gloves.
2. When storing at room temperature, the container needs to be kept sealed to avoid reaction with moisture in the air.
3. Open flames and high temperatures should be avoided during use and storage to prevent fire and explosion.
4. Avoid contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
PACKAGE
250KG/Barrel
CHEMICAL PROPERTIES
Ethyl difluorobromoacetate is a colorless and transparent liquid. It is an important organic synthesis intermediate and is often used in the synthesis of drugs and pesticides with biological enzyme functions. In ethyl difluorobromoacetate, CF2 with strong biological activity is introduced into the compound by replacing the bromine atom. The fluorine in the α position of these compounds increases the electrophilicity of the carbonyl group, which increases the active site of biological enzymes.
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