2-Bromo-5-Fluorobenzaldehyde CAS 94569-84-3 Assay ≥98.0% Factory High Quality

Short Description:

Chemical Name: 2-Bromo-5-Fluorobenzaldehyde 

CAS: 94569-84-3

Assay: ≥98.0%

Appearance: Light Yellow Crystal

High Quality, Commercialized Production

Inquiry: alvin@ruifuchem.com


Product Detail

Related Products

Product Tags

Description:

Manufacturer Supply with High Purity and Stable Quality
Chemical Name: 2-Bromo-5-Fluorobenzaldehyde 
CAS: 94569-84-3 
High Quality, Commercialized Production

Chemical Properties:

Chemical Name 2-Bromo-5-Fluorobenzaldehyde
CAS Number 94569-84-3
CAT Number RF-PI325
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C7H4BrFO
Molecular Weight 203.01
Density 1.7±0.1 g/cm3
Boiling Point 225.8±20.0℃ at 760 mmHg
Solubility Soluble in Methanol
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance Light Yellow Crystal
Water <0.50%
Melting Point 51.0~56.0℃
Assay  ≥98.0% 
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Package & Storage:

Package: Bottle, Aluminum foil bag, Cardboard drum, 25kg/Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

Advantages:

1

FAQ:

Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 2-Bromo-5-Fluorobenzaldehyde (CAS: 94569-84-3) with high quality, widely used in organic synthesis, synthesis of pharmaceutical intermediates and Active Pharmaceutical Ingredient (API) synthesis. 2-Bromo-5-Fluorobenzaldehyde is used as Tavaborole intermediate and has been used as a reactant for the preparation of pyridopyrimidinediones. 2-Bromo-5-fluorobenzaldehyde is used as a precursor for the synthesis of 5-fluoro-3-substituted benzoxaboroles, which is used in material science as molecular receptors, building block in crystal engineering, as steroid conjugates for molecular imprinting, dyes and biosensors of alpha hydroxyl carboxylic acids. It is also used in the synthesis of 5-arylindazolo[3,2-b]quinazolin-7(5H)-one by reacting with 2-amino-N′-arylbenzohydrazide in the presence of Copper(I) bromide by the Ullmann-type reaction. 2-Bromo-5-fluorobenzaldehyde can be prepared by reacting 2-bromo-5-fluorotoluene with N-bromosuccinimide. Its crystals exhibit monoclinic crystal system and space group P21/c.  

  • Write your message here and send it to us