Tosyl isocyanate

Base Information

  • PRODUCT:Tosyl isocyanate
  • CAS.:4083-64-1
  • MF:C8H7NO3S
  • Molecular Weight:197.214
  • Purity:99%

Product Details

CAS: 4083-64-1

MF: C8H7NO3S

Appearance: clear liquid

Chinese factory supply Tosyl isocyanate 4083-64-1 in stock with high standard

  • Molecular Formula:C8H7NO3S
  • Molecular Weight:197.214
  • Appearance/Colour:clear liquid 
  • Vapor Pressure:1 mm Hg ( 100 °C) 
  • Melting Point:5°C 
  • Refractive Index:1.5340 
  • Boiling Point:288.8 °C at 760 mmHg 
  • Flash Point:128.5 °C 
  • PSA:71.95000 
  • Density:1.27 g/cm3 
  • LogP:2.10030 

Tosyl isocyanate(Cas 4083-64-1) Usage

Chemical Description

Tosyl isocyanate is an organic compound with the formula CH3C6H4SO2NCO.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 9609, 1994 DOI: 10.1016/0040-4039(94)88523-0

Hazard

Moderately toxic by ingestion. Low toxicity by inhalation. A mild skin and moderate eye irritant.

Synthesis

Add the organic azide (0.75 mmol), Pd(OAc)2 (5.6 mg, 5 mol%) to an oven-dried Schlenk tube (10 mL). Purge the tube and backfill with CO (three cycles) from a balloon. Inject anhydrous MeCN (3.0 mL) into the tube. Stir at 80°C for 4 h under CO atmosphere (balloon). Concentrate the mixture under reduced pressure. Purify the residue by column chromatography (petroleum ether/EtOAc 3:1.-.1:1).

General Description

p-Toluenesulfonyl isocyanate undergoes palladium-catalyzed bis-allylation reaction with allylstannanes and allyl chlorides.

InChI:InChI=1/C8H7NO3S/c1-7-2-4-8(5-3-7)13(11,12)9-6-10/h2-5H,1H3

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4083-64-1 Relevant articles

Carbonylation of Selenilimines to Arylsulfonyl Isocyanates

Besenyei, Gabor,Nemeth, Sandor,Simandi, Laszlo I.

, p. 9609 - 9610 (1994)

Selenilimines of general formula ArSO2N=...

Intermolecular C-H Amidation of Alkenes with Carbon Monoxide and Azides via Tandem Palladium Catalysis

Gu, Zheng-Yang,Wu, Yang,Jin, Feng,Bao, Xiaoguang,Xia, Ji-Bao

supporting information, p. 3361 - 3371 (2021/04/09)

An atom- and step-economic intermolecula...

Pd-catalyzed amidation of 1,3-diketones with CO and azidesviaa nitrene intermediate

Gu, Zheng-Yang,Chen, Jie,Xia, Ji-Bao

supporting information, p. 11437 - 11440 (2020/10/12)

An efficient Pd-catalyzed amidation of 1...

Synthesis method of tertiary butyl isocyanate

-

Paragraph 0053-0088, (2018/09/08)

The invention relates to a synthesis met...

Syntheses of isocyanates via amines and carbonyl fluoride

Quan, Hengdao,Zhang, Ni,Zhou, Xiaomeng,Qian, Hua,Sekiya, Akira

supporting information, p. 26 - 30 (2015/06/08)

Isocyanates are widely used in many diff...

4083-64-1 Process route

p-toluenesulfonylcarbamyl fluoride

p-toluenesulfonylcarbamyl fluoride

Tosyl isocyanate
4083-64-1

Tosyl isocyanate

Conditions
Conditions Yield
In toluene; at 140 ℃; for 2h; Glovebox;
84%
phosgene
75-44-5

phosgene

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

Tosyl isocyanate
4083-64-1

Tosyl isocyanate

Conditions
Conditions Yield
With 1,2,3-trichlorobenzene;
 
In 5,5-dimethyl-1,3-cyclohexadiene; at 100 ℃; for 2h; Time; Temperature; Solvent; Inert atmosphere;
 

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