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CAS RN: 430-67-1 | Product Number: D4758

2,2-Difluoroethylamine


Purity: >98.0%(GC)(T)
Synonyms:
Product Documents:
1G
18,00 €
Contact Us ≥80 
5G
56,00 €
3   ≥100 

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Product Number D4758
Purity / Analysis Method >98.0%(GC)(T)
Molecular Formula / Molecular Weight C__2H__5F__2N = 81.07 
Physical State (20 deg.C) Liquid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Air Sensitive
CAS RN 430-67-1
Reaxys Registry Number 1731615
PubChem Substance ID 253661046
MDL Number

MFCD00798137

Specifications
Appearance Colorless to Yellow clear liquid
Purity(GC) min. 98.0 %
Purity(Neutralization titration) min. 98.0 %
NMR confirm to structure
Properties (reference)
Boiling Point 68 °C
Flash point -34 °C
Specific Gravity (20/20) 1.17
Refractive Index 1.34
GHS
Pictogram Pictogram Pictogram
Signal Word Danger
Hazard Statements H314 : Causes severe skin burns and eye damage.
H225 : Highly flammable liquid and vapour.
Precautionary Statements P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish.
P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water.
P304 + P340 + P310 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor.
P305 + P351 + P338 + P310 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor.
Related Laws:
Transport Information:
UN Number UN2733
Class 3 / 8
Packing Group II
HS Number 2914790090
Application
Reagents for Difluoromethylation (Precursor to difluoromethyl diazomethane)

D4758

Typical Procedure:
To a stirred solution of 2,2-difluoroethylamine (193 mg, 2.38 mmol, 2.0 eq.) in CHCl3 (20 mL), tert-butyl nitrite (294 mg, 2.86 mmol, 2.4 eq.) and acetic acid (28 mg, 0.48 mmol, 0.4 eq.) are added. The solution is heated at reflux whereas the mixture becomes deeply yellow. After 10 min, the heating is stopped, and the reaction mixture is cooled down to a room temperature by external water bath. Methyl propiolate (100 mg, 1.19 mmol, 1.0 eq.) is added at once. The reaction mixture is left at room temperature for 24 h. The solvent is evaporated under vacuum. The formed oily residue is purified by column chromatography on silica gel using hexane-EtOAc (2:1) as an eluent, to afford the pure product (159 mg, 0.90 mmol, 76% yield) as a colorless solid.

References


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
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