fluoromethane-13c

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Names

[ CAS No. ]:
20666-44-8

[ Name ]:
fluoromethane-13c

[Synonym ]:
<13C>-methyl fluoride
<13C>-Methylfluorid
methyl fluoride-13C
MFCD00083967

Chemical & Physical Properties

[ Density]:
1.231 (vs air)

[ Boiling Point ]:
-77.9ºC(lit.)

[ Melting Point ]:
-141.8ºC(lit.)

[ Molecular Formula ]:
CH3F

[ Molecular Weight ]:
35.02560

[ Exact Mass ]:
35.02520

[ LogP ]:
0.58570

[ Index of Refraction ]:
1.212

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS04

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H220-H280

[ Precautionary Statements ]:
P210-P377-P381-P410 + P403

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US)

[ Hazard Codes ]:
F+: Highly flammable;

[ Risk Phrases ]:
R12

[ Safety Phrases ]:
16-33

[ RIDADR ]:
UN 2454 2.1

Articles

Theoretical studies on identity S(N)2 reactions of lithium halide and methyl halide: a microhydration model.

J. Mol. Model. 16(12) , 1931-7, (2010)

Reactions of lithium halide (LiX, X = F, Cl, Br and I) and methyl halide (CH₃X, X = F, Cl, Br and I) have been investigated at the B3LYP/6-31G(d) level of theory using the microhydration model. Beginn...

A-band methyl halide dissociation via electronic curve crossing as studied by electron energy loss spectroscopy.

J. Chem. Phys. 133(5) , 054304, (2010)

Excitation of the A-band low-lying electronic states in the methyl halides, CH(3)I, CH(3)Br, CH(3)Cl, and CH(3)F, has been investigated for the (n-->sigma*) transitions, using electron energy loss spe...

Near-thermal reactions of Au(+)(1S,3D) with CH3X (X = F,Cl).

J. Phys. Chem. A 116(3) , 943-51, (2012)

Reactions of Au(+)((1)S) and Au(+)((3)D) with CH(3)F and CH(3)Cl have been carried out in a drift cell in He at a pressure of 3.5 Torr at both room temperature and reduced temperatures in order to exp...


More Articles


Related Compounds

  • fluoromethane,helium
  • fluoromethane
  • fluoromethane hydrofluoride
  • fluoromethane,hydrate
  • fluoromethane-d1
  • methanol-13c
  • N-(2-(3-(4-fluorophenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-3-(4-oxoquinazolin-3(4H)-yl)propanamide
  • N-(2-(3-(4-methoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)isoxazole-5-carboxamide
  • ethyl 4-(2-(5-amino-3-(methylthio)-4-tosyl-1H-pyrazol-1-yl)acetamido)benzoate
  • N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-2-((4-fluorophenyl)thio)acetamide
  • 2-(benzo[d]isoxazol-3-yl)-N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)acetamide
  • N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-2,5-dimethylfuran-3-carboxamide
  • N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-1-(methylsulfonyl)piperidine-4-carboxamide
  • N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-3-(1H-tetrazol-1-yl)benzamide
  • 2-(5-amino-4-(3-(benzo[d][1,3]dioxol-5-yl)-1,2,4-oxadiazol-5-yl)-3-(methylthio)-1H-pyrazol-1-yl)-N-phenylacetamide
  • N-(2-(3-(4-ethoxyphenyl)-6-oxopyridazin-1(6H)-yl)ethyl)-1-methyl-2-oxo-1,2-dihydropyridine-3-carboxamide
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