CAS 36635-61-7
:Tosylmethyl isocyanide
Description:
Tosylmethyl isocyanide, also known as isocyanomethyl tosylate, is an organic compound characterized by its isocyanide functional group attached to a tosyl (p-toluenesulfonyl) moiety. It typically appears as a colorless to pale yellow liquid and is known for its strong and often unpleasant odor, which is characteristic of isocyanides. This compound is notable for its reactivity, particularly in nucleophilic addition reactions, making it useful in organic synthesis, especially in the formation of various nitrogen-containing compounds. Tosylmethyl isocyanide can participate in cycloaddition reactions and is often employed in the synthesis of heterocycles. It is important to handle this compound with care due to its potential toxicity and irritant properties. Additionally, it is soluble in organic solvents, which facilitates its use in various chemical reactions. As with many isocyanides, safety precautions should be taken to avoid inhalation or skin contact, and it should be stored in a cool, dry place away from incompatible substances.
Formula:C9H9NO2S
InChI:InChI=1S/C9H9NO2S/c1-8-3-5-9(6-4-8)13(11,12)7-10-2/h3-6H,7H2,1H3
InChI key:InChIKey=CFOAUYCPAUGDFF-UHFFFAOYSA-N
SMILES:S(C[N+]#[C-])(=O)(=O)C1=CC=C(C)C=C1
Synonyms:- (4-Methylphenylsulfonyl)methyl isocyanide
- (P-Tolylsulfonyl)Methyl Isocyanide
- 1-(Isocyanomethanesulfonyl)-4-methylbenzene
- 1-[(Isocyanomethyl)Sulfonyl]-4-Methyl-Benzen
- 1-[(Isocyanomethyl)Sulfonyl]-4-Methylbenzene
- 4-Toluenesulfonylmethyl Isocyanide
- 4-Toluenesulfonylmethylisocyanide
- 4-Toluenesulphonylmethyl Isocyanide
- 4-Toluensulfonylmethyl Isocyanide
- 4-Tolylsulfonylmethyl isocyanide
- Benzene, 1-[(Isocyanomethyl)Sulfonyl]-4-Methyl-
- Isocyanomethyl p-tolyl sulfone
- Labotest-Bb Lt00159629
- Methylidyne[[(4-Methylphenyl)Sulfonyl]Methyl]Ammonium
- NSC 631633
- P-Toluenesulfonyl Methylisocyanide
- P-Toluenesulfonylmethyl Isocyande
- P-Toluenesulfonylmethyl Isocyanide
- Tosmic
- Tosylmethylisocyanide
- [(4-Methylphenyl)Sulfonyl]Acetonitrile
- p-Toluenesulfonylmethylisonitrile
- p-Tosylmethyl isocyanide
- p-Tosylmethyl isonitrile
- See more synonyms
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Found 9 products.
p-Toluenesulfonylmethyl Isocyanide
CAS:Formula:C9H9NO2SPurity:>98.0%(HPLC)(N)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:195.24p-Toluenesulfonylmethyl isocyanide, 97%
CAS:<p>p-Toluenesulfonylmethyl isocyanide is a synthetic reagent used in the synthesis of triplet drugs with the 1,3,5-trioxazatriquinane skeleton, pyrroles, oxazoles and in imidazoles. It serves as an isonitrile component in a diastereoselective Passerini reaction. Furthermore, it is used in the Van Leuse</p>Formula:C9H9NO2SPurity:97%Color and Shape:White to cream or pale yellow to pale brown, Crystalline powder or powderMolecular weight:195.24Isocyanomethyl 4-methylphenyl sulphone
CAS:Isocyanomethyl 4-methylphenyl sulphoneFormula:C9H9NO2SPurity:98%Color and Shape: faint orange to light yellow crystalline solidMolecular weight:195.23826g/mol4-Toluenesulfonylmethylisocyanide
CAS:Formula:C9H9NO2SPurity:98.0%Color and Shape:Chunks,Crystalline PowderMolecular weight:195.24p-Toluenesulfonylmethyl isocyanide
CAS:Formula:C9H9NO2SPurity:≥ 98.0%Color and Shape:White to yellow, orange, beige or brown powder or crystalsMolecular weight:195.24Tosylmethyl Isocyanide
CAS:Controlled ProductFormula:C9H9NO2SColor and Shape:NeatMolecular weight:195.244-Toluenesulfonylmethylisonitrile
CAS:<p>4-Toluenesulfonylmethylisonitrile is a potent antagonist of the malonic acid receptor that has been shown to be reactive. It is synthesized by reacting methyl ketones with trifluoroacetic acid and nitrogen gas in the presence of a catalyst. The reaction mechanism has been studied using gravimetric analysis and the thermodynamic data have been calculated for fatty acids. 4-Toluenesulfonylmethylisonitrile can be used to make esters.</p>Formula:C9H9NO2SPurity:Min. 95%Color and Shape:Off-White To Yellow SolidMolecular weight:195.24 g/mol
