146328-85-0

• 

• Basic information

  1. Product Name: 5-Bromo-2-fluorobenzoic acid
  2. Synonyms: RARECHEM AL BO 0757;2-FLUORO-5-BROMOBENZOIC ACID;5-BROMO-2-FLUOROBENZOIC ACID;BUTTPARK 19\01-67;5-Bromo-2-Fluorobenzoic Acid 2-Fluoro-5-Bromobenzoic Acid;5-Bromo-2-fluorobenzoic;5-Bromo-2-fluorobenzoic acid 97%;5-Bromo-2-fluorobenzoicacid97%
  3. CAS NO:146328-85-0
  4. Molecular Formula: C₇H₄BrFO₂
  5. Molecular Weight: 219.01
  6. EINECS: 604-519-9
  7. Product Categories: Fluorin-contained Benzoic acid series;blocks;Bromides;Carboxes;FluoroCompounds;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Benzoic acid;Miscellaneous;Acids & Esters;Bromine Compounds;Fluorine Compounds;C7;Carbonyl Compounds;Carboxylic Acids;Benzoic acid series;Fluorine series
  8. Mol File: 146328-85-0.mol
  9. Article Data: 11

• Chemical Properties

  1. Melting Point: 141-145 °C(lit.)
  2. Boiling Point: 296.5 °C at 760 mmHg
  3. Flash Point: 133.1 °C
  4. Appearance: /
  5. Density: 1.789 g/cm³
  6. Vapor Pressure: 0.000644mmHg at 25°C
  7. Refractive Index: N/A
  8. Storage Temp.: Sealed in dry,Room Temperature
  9. Solubility: N/A
  10. PKA: 2.88±0.10(Predicted)
  11. Water Solubility: Slightly soluble in water.
  12. CAS DataBase Reference: 5-Bromo-2-fluorobenzoic acid(CAS DataBase Reference)
  13. NIST Chemistry Reference: 5-Bromo-2-fluorobenzoic acid(146328-85-0)
  14. EPA Substance Registry System: 5-Bromo-2-fluorobenzoic acid(146328-85-0)

• Safety Data

  1. Hazard Codes: Xn,Xi
  2. Statements: 22
  3. Safety Statements: 26
  4. RIDADR: UN 2811 6.1/PG 3
  5. WGK Germany: 3
  6. RTECS:
  7. HazardClass: IRRITANT
  8. PackingGroup: Ⅲ
  9. Hazardous Substances Data: 146328-85-0(Hazardous Substances Data)

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• 5-Bromo-2-fluorobenzoic acid

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• USD $ 3.0-3.0 / Kilogram

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• Dayang Chem (Hangzhou) Co.,Ltd.
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• High quality 2-Fluoride-5-Bromine Benzoic Acids supplier in China

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• 5-Bromo-2-fluorobenzoic acid

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• 5-Bromo-2-fluorobenzoic acid

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• 2-fluoride-5-bromine benzoic acids

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146328-85-0 Usage

Description

5-Bromo-2-fluorobenzoic acid is an organic compound characterized by the presence of a bromine atom at the 5th position and a fluorine atom at the 2nd position on a benzoic acid backbone. It is a white solid with specific chemical properties that make it a valuable intermediate in the synthesis of various pharmaceuticals and organic compounds.

Uses

Used in Pharmaceutical Industry:
5-Bromo-2-fluorobenzoic acid is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure allows for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic chemistry, 5-Bromo-2-fluorobenzoic acid serves as an important intermediate for the synthesis of various organic compounds. Its bromine and fluorine substituents can be utilized in a variety of chemical reactions, enabling the production of diverse molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 146328-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,2 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 146328-85:
(8*1)+(7*4)+(6*6)+(5*3)+(4*2)+(3*8)+(2*8)+(1*5)=140
140 % 10 = 0
So 146328-85-0 is a valid CAS Registry Number.

InChI:InChI=1/C7H4BrFO2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,(H,10,11)/p-1

146328-85-0 Well-known Company Product Price

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• Alfa Aesar

• (H60595)  5-Bromo-2-fluorobenzoic acid, 97%   

• 146328-85-0

• 1g

• 187.0CNY

• Detail

• Alfa Aesar

• (H60595)  5-Bromo-2-fluorobenzoic acid, 97%   

• 146328-85-0

• 5g

• 777.0CNY

• Detail

146328-85-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name	5-Bromo-2-fluorobenzoic acid

1.2 Other means of identification

Product number	-
Other names	5-BroMo-2-fluorobenzoic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:146328-85-0 SDS

146328-85-0Upstream product

• 124-38-9 carbon dioxide 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 445-29-4 o-fluoro-benzoic acid 
• 93777-26-5 5-bromo-2-fluorobenzaldehyde 

146328-85-0Downstream Products

• 935285-60-2 tert-butyl (5-bromo-2-fluorophenyl)carbamate 
• 247570-14-5 5-bromo-N-(4-chloro-3-methoxybenzyl)-2-fluorobenzamide 
• 247568-34-9 2-fluoro-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 
• 247569-37-5 5-bromo-N-(3,4-dimethoxybenzyl)-2-fluorobenzamide 
• 57381-59-6 methyl 2-fluoro-5-bromobenzoate 
• 146328-84-9 4-fluoro-[1,1'-biphenyl]-3-carboxylic acid 
• 552331-21-2 (5-bromo-2-fluorophenyl)(1H-pyrrol-2-yl)methanone 
• 773140-42-4 2-bromo-5-fluorobenzoyl chloride 
• 1266785-76-5 N-[(RS)-1-(5-bromo-2-fluoro-phenyl)-2-hydroxy-1-methyl-ethyl]-3-phenyl-acrylamide 
• 1266785-74-3 (2RS)-bromo-N-[(RS)-1-(5-bromo-2-fluoro-phenyl)-2-hydroxy-1-methyl-ethyl]-3-phenyl-propionamide 
• 453566-35-3 3-(pyridin-2-yl)-5-(5-bromo-2-fluorophenyl)-1,2,4-oxadiazole 
• 940284-95-7 C₁₃H₁₇BrN₂O₂ 
• 247568-30-5 (R)-5-Acetyl-N-(4-chloro-3-methoxybenzyl)-2-(2-hydroxy-1-methylethylamino)benzamide 
• 247568-36-1 (S)-2-[1-(hydroxymethyl)propylamino]-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide 

146328-85-0Relevant articles and documents

Synthesis method of 2-halo-5-bromobenzoic acid

-

Paragraph 0038-0042, (2019/10/01)

The invention discloses a synthesis method of 2-halo-5-bromobenzoic acid. The method comprises the following steps of under the action of sulfuric acid, carrying out a bromination reaction on o-halo-benzoic acid and NBS in an organic solvent, and after the reaction is finished, carrying out posttreatment to obtain 2-halo-5-bromobenzoic acid. The method has the advantages of being short in reactionroute, simple in operation, environmentally friendly, safe and economical and has a broad application prospect.

TRIAZOLONES DERIVATIVES FOR USE IN THE TREATMENT, AMELIORATION OR PREVENTION OF A VIRAL DISEASE

-

Page/Page column 54, (2017/04/18)

The present invention relates to a compound having the general formula (I), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph, prodrug, tautomer, racemate, codrug, cocrystal, enantiomer, or diastereomer or mixture thereof, which is useful in treating, ameloriating or preventing a viral disease. Furthermore, specific combination therapies are disclosed.

Synthesis and structural characterization of new phosphinooxazoline complexes of iron

Sedinkin, Sergey L.,Rath, Nigam P.,Bauer, Eike B.

, p. 3081 - 3091 (2008/12/22)

The first phosphinooxazoline chelate complexes of iron were synthesized, and their structural and electronic properties were studied. The known phosphinooxazolines 2-(2-(diphenylphosphino)phenyl)-4,5-dihydrooxazole (7a), 2-(2-(diphenylphosphino)phenyl)-4,

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