Tosylmethyl isocyanide structure
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Common Name | Tosylmethyl isocyanide | ||
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CAS Number | 36635-61-7 | Molecular Weight | 195.238 | |
Density | 1.24 g/cm3 | Boiling Point | 400.9ºC at 760 mmHg | |
Molecular Formula | C9H9NO2S | Melting Point | 109-113 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 196.3ºC | |
Symbol |
GHS06 |
Signal Word | Danger |
Name | Tosylmethyl isocyanide |
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Synonym | More Synonyms |
Density | 1.24 g/cm3 |
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Boiling Point | 400.9ºC at 760 mmHg |
Melting Point | 109-113 °C(lit.) |
Molecular Formula | C9H9NO2S |
Molecular Weight | 195.238 |
Flash Point | 196.3ºC |
Exact Mass | 195.035400 |
PSA | 42.52000 |
LogP | 1.95700 |
Storage condition | -20°C |
Water Solubility | insoluble |
Symbol |
GHS06 |
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Signal Word | Danger |
Hazard Statements | H301 + H311 + H331 |
Precautionary Statements | P261-P280-P301 + P310-P311 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type P2 (EN 143) respirator cartridges |
Hazard Codes | T:Toxic |
Risk Phrases | R23/24/25 |
Safety Phrases | S36/37-S45-S38-S36/37/39-S28A |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 29299000 |
HS Code | 2926909090 |
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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% |
Microwave-assisted synthesis of imidazoles: reaction of p-toluenesulfonylmethyl isocyanide and polymer-bound imines.
Bioorg. Med. Chem. Lett. 15(16) , 3717-9, (2005) A convenient method for the synthesis of 1,5-disubstituted imidazoles has been developed on a polymeric support using base-promoted 1,3-dipolar cycloaddition reaction of p-toluenesulfonylmethyl isocya... |
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Synthesis of novel triplet drugs with 1,3,5-trioxazatriquinane skeletons and their pharmacologies. Part 2: Synthesis of novel triplet drugs with the epoxymethano structure (capped homotriplet).
Bioorg. Med. Chem. Lett. 21(20) , 6198-202, (2011) An improved synthetic method for triplet drugs with the 1,3,5-trioxazatriquinane skeleton was developed that used p-toluenesulfonylmethyl isocyanide (TosMIC) instead of 1,3-dithiane. Using the improve... |
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Alkyl and aromatic isocyanide binding to haem complexes.
Biochem. J. 262(3) , 959-63, (1989) Equilibrium constants for the binding of ethyl (EIC), n-butyl (BIC), p-toluenesulphonylmethyl (TMIC) and 2,6-dimethylphenyl isocyanides (DIMPI) to an imidazole-haem complex in toluene and aqueous dete... |
TosMICTosylmethyl Isocyanide |
4-toluene-sulfonylmethyl isocyanide |
(p-Tolylsulfonyl)methyl isocyanide |
Tosylmethy isocyanide |
Tosylmethylisocyanide |
Isocyanomethyl 4-methylphenyl sulfone |
Benzene, 1-((isocyanomethyl)sulfonyl)-4-methyl- |
p-Toluenesulfonylmethyl isocyanide |
1-[(Isocyanomethyl)sulfonyl]-4-methylbenzene |
4-Toluenesulfonylmethyl isocyanide |
P-tolysulfonylmethylisocyanide |
p-tosylmethyl isocyanide |
4-Toluenesulfonylmethylisocyanide |
TOSMIC |
EINECS 253-140-1 |
p-Toluenesulfonyl Isocyanide |
Tosylmethyl isocyani |
MFCD00000005 |
Benzene, 1-[(isocyanomethyl)sulfonyl]-4-methyl- |
IsocyanoMethyl p-Tolyl Sulfone |
1-[(Isocyanmethyl)sulfonyl]-4-methylbenzol |
4-Toluenesulphonylmethyl Isocyanide |