Cyanomethyl benzenesulfonate

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Names

[ CAS No. ]:
10531-13-2

[ Name ]:
Cyanomethyl benzenesulfonate

[Synonym ]:
MFCD00007547
Acetonitrile,((phenylsulfonyl)oxy)
phenylsulfonyloxyacetonitrile
benzenesulfonyloxy-acetonitrile
Cyanomethylbenzenesulfonate
EINECS 234-093-6
Cyanomethyl benzenesulphonate
Benzolsulfonyloxy-acetonitril

Chemical & Physical Properties

[ Density]:
1.309

[ Boiling Point ]:
142-146ºC (1 mmHg)

[ Molecular Formula ]:
C8H7NO3S

[ Molecular Weight ]:
197.21100

[ Flash Point ]:
113ºC

[ Exact Mass ]:
197.01500

[ PSA ]:
75.54000

[ LogP ]:
1.99628

[ Vapour Pressure ]:
7.27E-05mmHg at 25°C

[ Index of Refraction ]:
1.523

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302 + H312 + H332-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

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

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22;R34

[ Safety Phrases ]:
26-27-36/37/39

[ RIDADR ]:
UN 1760

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ HS Code ]:
2926909090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Separation of aromatic hydrophobic sulfonates by micellar electrokinetic chromatography.

J. Chromatogr. A. 1161(1) , 322-326, (2007)

Two different buffer systems for the separation of 12 aromatic hydrophobic sulfonates by micellar electrokinetic chromatography (MEKC) were developed. The following buffer systems were used: aqueous p...

[Studies on application of cyanomethyl benzenesulfonate as a new cyanomethylating agent. I. Cyanomethyl esters of arylsulfonic acids].

Acta Pol. Pharm. 23(5) , 417-23, (1966)

Synthesis of nido-and closo-arsacarboranes. Smith J, et al.

Inorg. Chem. 13(10) , 2312-2316, (1974)


More Articles

Related Compounds

  • cyanomethyl-diethyl-methylazanium,iodide
  • cyanomethyl(2,4-dimethylpentan-2-yl)azanium,chloride
  • Cyanomethyl p-toluenesulfonate
  • Cyanomethyl dimethylcarbamodithioate
  • cyanomethyl-diethyl-methylazanium,bromide
  • cyanomethyl-hexa-1,5-dien-3-yl-dimethylazanium,chloride
  • N-[1-(4-aminophenyl)-1,3-dihydroxypropan-2-yl]propanamide
  • 4-hydroxy-1-(4-methoxybenzyl)-6-methylpyridin-2(1H)-one
  • 3-((2-chlorophenyl)(4-(pyridin-2-yl)piperazin-1-yl)methyl)-1-ethyl-4-hydroxy-6-methylpyridin-2(1H)-one
  • Ethyl 4-((3-chlorophenyl)(1-ethyl-4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)piperazine-1-carboxylate
  • 3-((3-chlorophenyl)(4-(2-fluorophenyl)piperazin-1-yl)methyl)-1-ethyl-4-hydroxy-6-methylpyridin-2(1H)-one
  • 1-ethyl-3-((4-fluorophenyl)(4-(pyridin-2-yl)piperazin-1-yl)methyl)-4-hydroxy-6-methylpyridin-2(1H)-one
  • Ethyl 4-((1-ethyl-4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)(p-tolyl)methyl)piperazine-1-carboxylate
  • 1-ethyl-3-((4-(2-fluorophenyl)piperazin-1-yl)(p-tolyl)methyl)-4-hydroxy-6-methylpyridin-2(1H)-one
  • 3-((4-benzylpiperidin-1-yl)(pyridin-3-yl)methyl)-1-ethyl-4-hydroxy-6-methylpyridin-2(1H)-one
  • 4-hydroxy-1-(2-methoxyethyl)-6-methyl-3-((4-(pyridin-2-yl)piperazin-1-yl)(p-tolyl)methyl)pyridin-2(1H)-one
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