Tributyl(2-furyl)stannane

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Names

[ CAS No. ]:
118486-94-5

[ Name ]:
Tributyl(2-furyl)stannane

[Synonym ]:
Tributyl(2-furyl)stannane
tributyl(furan-2-yl)stannane
Stannane, tributyl-2-furanyl-
MFCD00192512

Chemical & Physical Properties

[ Density]:
1.134 g/mL at 25 °C(lit.)

[ Boiling Point ]:
343.1±34.0 °C at 760 mmHg

[ Molecular Formula ]:
C16H30OSn

[ Molecular Weight ]:
357.119

[ Flash Point ]:
161.3±25.7 °C

[ Exact Mass ]:
358.131866

[ PSA ]:
13.14000

[ LogP ]:
9.18

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.494(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS06, GHS08, GHS09

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H301-H312-H315-H319-H372-H410

[ Precautionary Statements ]:
P273-P280-P301 + P310-P305 + P351 + P338-P314-P501

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
T:Toxic;N:Dangerousfortheenvironment;

[ Risk Phrases ]:
R21;R25;R36/38;R48/23/25;R50/53

[ Safety Phrases ]:
S35-S36/37/39-S45-S60-S61

[ RIDADR ]:
UN 2788 6.1/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1(b)

[ HS Code ]:
2932190090

Synthetic Route

Precursor & DownStream

Precursor

  • Furan
  • Chlorotributyltin

DownStream

  • 4-FURAN-2-YL-BENZOIC ACID
  • 2-FURAN-2-YL-PHENYLAMINE
  • 4-FURAN-2-YL-BENZOIC ACID METHYL ESTER
  • 2-furan-2-yl-benzoic acid methyl ester
  • Aids186752
  • 2-Furancarboxamide,N-(3-chlorophenyl)-
  • 2-[4-(trifluoromethyl)phenyl]furan
  • 1-Methyl-2-phenylindole
  • 3-FURAN-2-YL-BENZALDEHYDE
  • [3-(2-FURYL)PHENYL]METHANOL

Customs

[ HS Code ]: 2932190090

[ Summary ]:
2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

Phenoxazine based units--synthesis, photophysics and electrochemistry.

J. Fluoresc. 21 , 169-78, (2011)

A few new phenoxazine-based conjugated monomers were synthesized, characterized, and successfully used as semiconducting materials. The phenoxazine-based oligomers have low ionization potentials or hi...


More Articles


Related Compounds

  • tributyl-(2-methylphenoxy)stannane
  • Tributyl(2-methoxyphenyl)stannane
  • Tributyl(selenophen-2-yl)stannane
  • tributyl(2-ethylhexoxy)stannane
  • tributyl-(2-ethylsulfanylphenyl)stannane
  • tributyl-(2-methylsulfanylphenyl)stannane
  • 1-(2-Phenylethynyl)cyclohexanamine
  • (E)-N-[2-[4-[bis(4-fluorophenyl)methyl]piperazin-1-yl]-2-oxoethyl]-N-methyl-2-phenylethenesulfonamide
  • Ethyl 2-(triphenylphosphoranylidene)hexanoate
  • N,N,2-Trimethyl-5-phenyl-4-thiazolecarboxamide
  • 6-chloro-N-({1-[(2-chlorophenyl)methyl]-3-phenyl-1H-pyrazol-4-yl}methyl)-N-methylpyridine-3-sulfonamide
  • Methyl 5-bromonicotinimidate
  • 2-{1-[(tert-butoxy)carbonyl]-1H-imidazol-4-yl}-2-hydroxyacetic acid
  • Ethyl 2-amino-4-methyl-3-oxopentanoate
  • (3aS,3bR,5aR,9aR,9bS,11aS)-1-iodo-9a,11a-dimethyl-3,3a,3b,4,5,5a,6,8,9,9b,10,11-dodecahydroindeno[5,4-f]quinolin-7-one
  • 2-(3-Bromophenyl)-4,5-dihydro-1,3-oxazole
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