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CAS RN: 36635-66-2 | Product Number: T3157

α-(p-Toluenesulfonyl)benzyl Isocyanide


Purity: >98.0%(HPLC)(N)
Synonyms:
  • α-Tosylbenzyl Isocyanide
Product Documents:
1G
298,00 €
1   7  
5G
1 399,00 €
1   5  

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Product Number T3157
Purity / Analysis Method >98.0%(HPLC)(N)
Molecular Formula / Molecular Weight C__1__5H__1__3NO__2S = 271.33 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 36635-66-2
Reaxys Registry Number 2291401
PubChem Substance ID 354333607
MDL Number

MFCD04114776

Specifications
Appearance White to Light yellow to Light orange powder to crystal
Purity(HPLC) min. 98.0 area%
Purity(with Total Nitrogen) min. 98.0 %
Properties (reference)
Melting Point 106 °C(dec.)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H302 + H312 + H332 : Harmful if swallowed, in contact with skin or if inhaled.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P261 : Avoid breathing dust.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P302 + P352 + P312 : IF ON SKIN: Wash with plenty of water. Call a POISON CENTER/doctor if you feel unwell.
P304 + P340 + P312 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Call a POISON CENTER/doctor if you feel unwell.
Related Laws:
Transport Information:
HS Number 2930909899
Application
p-Toluenesulfonylmethyl Isocyanide Derivatives Effective in the Construction of Heterocyclic Compounds

T3157,T1046

Experimental procedure: To 4-pentenal (3, 252 mg, 3.0 mmol) in DMF (3 mL) is added allylamine (2, 171 mg, 3.0 mmol), and the reaction mixture is stirred at room temperature for 2.5 h. This is followed by the addition of α-(p-toluenesulfonyl)benzyl isocyanide (1, 543 mg, 2.0 mmol) and K2CO3 (276 mg, 2.0 mmol), and the reaction mixture is allowed to stir for an additional 17 h at room temperature. The reaction is quenched by the addition of water. The aqueous layer is extracted with EtOAc, dried (anhydrous MgSO4), concentrated, and purified by flash column chromatography (CH2Cl2:CH3OH:NH3 = 97:2.5:0.5) to afford 433 mg (91%) of 4 as an oil.

References


PubMed Literature


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