Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 459-46-1
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Plastic bottles, Plastic buckets
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS NO:: |
459-46-1 |
Appearance:: |
Colorless To Light Yellow Liquid |
Molecular Formula:: |
C7H6BrF |
Molecular Weight:: |
189.02500 |
EINECS NO:: |
207-291-5 |
MDL NO:: |
MFCD00000359 |
CAS NO:: |
459-46-1 |
Appearance:: |
Colorless To Light Yellow Liquid |
Molecular Formula:: |
C7H6BrF |
Molecular Weight:: |
189.02500 |
EINECS NO:: |
207-291-5 |
MDL NO:: |
MFCD00000359 |
Product Description:
Product Name: 4-Fluorobenzyl bromide CAS NO: 459-46-1
Synonyms:
4-Fluoro-1-(bromomethyl)benzene;
α-Bromo-4-fluorotoluene;
1-(Bromomethyl)-4-fluorobenzene, alpha-Bromo-4-fluorotoluene;
Chemical & Physical Properties:
Appearance: Colorless to light yellow liquid
Assay :≥99.0%
Density: 1.517
Boiling Point: 85℃ (15 mmHg)
Flash Point: 74.8℃
Refractive Index: 1.5464-1.5484
Sensitive: Lachrymatory
Stability: Stable at room temperature in closed containers under normal storage and handling conditions. Reacts with water to form toxic fumes.
Storage Condition: Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances. Store protected from moisture.
Vapor Pressure: 0.143mmHg at 25℃
Safety Information:
Hazard Class: 8
Safety Statements: S26-S36/37/39-S45
HS Code: 2903999090
Packing Group: III
WGK Germany: 3
RIDADR: UN 3265
Risk Statements: R34; R36
Hazard Code: C
4-Fluorobenzyl Bromide is a substituted benzyl bromide reagent used in the preparation of wide range of biologically active compounds such as bronchodialators, neurochemicals and antibacterials. 4-Fluorobenzyl bromide is an important intermediate in organic chemistry. 4-Fluorobenzyl bromide can be used as alkylating reagent to participate in the alkylation reaction with sulfamic esters (R-O-SO2-NH2) in liquid-liquid phase transfer conditions, resulting in the preparation of the N-dialkyled products or the corresponding ethers by scission of the O-SO2 bond, depending on the nature of R.4-Fluorobenzyl bromide can be used for the synthesis of glycyrrhetinic acid (GA) derivatives, which are slow-binding inhibitors of tyrosinase and have inhibitory effects on melanogenesis.
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