(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE

(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE Structure
CAS No.
36635-66-2
Chemical Name:
(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE
Synonyms
SKL019;A-TOSYLBENZYL ISOCYANIDE;alfa-Tosylbenzylisocyanide;ALPHA-TOSYLBENZYL ISOCYANIDE;(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE;a-(4-Tolylsulfonyl)benzylisocyanide;α-(p-Toluenesulfonyl)benzyl Isocyanide;α-(p-Toluenesulfonyl)benzyl Isocyanide;alpha-(p-Toluenesulfonyl)benzyl Isocyanide;alpha-(Toluene-4-sulphonyl)benzyl isocyanide
CBNumber:
CB8709143
Molecular Formula:
C15H13NO2S
Molecular Weight:
271.33
MOL File:
36635-66-2.mol
Modify Date:
2023/6/8 17:06:38

(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE Properties

Melting point 106 °C(dec.)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form powder to crystal
color White to Light yellow to Light orange

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H315-H319-H335
Precautionary statements  P260-P271-P280
Hazard Codes  Xi
Hazard Note  Irritant
HS Code  2930909899
NFPA 704
0
2 0

(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) T3157 α-(p-Toluenesulfonyl)benzyl Isocyanide 36635-66-2 1G ₹37900 2022-05-26 Buy
TCI Chemicals (India) T3157 α-(p-Toluenesulfonyl)benzyl Isocyanide 36635-66-2 5G ₹131100 2022-05-26 Buy
Product number Packaging Price Buy
T3157 1G ₹37900 Buy
T3157 5G ₹131100 Buy

(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE Chemical Properties,Uses,Production

Preparation

A 1-L, three-necked, roundbottomed flask fitted with an overhead stirrer, a 100 mL addition funnel, and a temperature probe was charged with THF (200 mL) and 1615 (27.6 g, 94.8 mmol). Phosphoryl chloride (17.7 mL, 190 mmol) was added and the resulting solution was stirred for 5 min at 25 C??. After cooling the solution to 0 C??, triethylamine (79.3 mL, 569 mmol) was added slowly over 30¨C45 min while keeping the internal reaction temperature below 10 C??. After the addition of triethylamine was complete, the reaction mixture was warmed to 5¨C10 C?? and maintained at this temperature for 30¨C45 min. Ethyl acetate (140 mL) and water (140 mL) were added sequentially to the reaction mixture, stirring was continued for 5 min, and then the mixture was transferred to a separatory funnel and the aqueous layer was removed. The organic layer was washed with water (2?á140 mL), saturated sodium hydrogen carbonate solution (140 mL), and brine (70 mL). The organic layer was transferred to a 500-mL, round-bottomed flask and concentrated on a rotary evaporator. The residue was diluted with 1-propanol (140 mL) and this solution was concentrated on a rotary evaporator to half of its original volume. The residue was cooled to 5¨C10 C?? for 30 min and the beige solid that crystallized was collected by filtration through a Buchner funnel. The filter cake was rinsed with 1-propanol (2?á75 mL). The beige solid was dried in vacuo for 3¨C4 h to give 18.1¨C19.7 g (70¨C 76%) of a-tosylbenzyl isocyanide 1616.
Structurally analogous to TosMIC 1600 is PhosMIC 1617, which has a phosphonate residue instead of a sulfonate residue. Some representatives have been described by Bartlett.36635-66-2 synthesis

(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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(1-PHENYL-1-TOSYL)METHYL ISOCYANIDE Spectrum

A-TOSYLBENZYL ISOCYANIDE ALPHA-TOSYLBENZYL ISOCYANIDE (1-PHENYL-1-TOSYL)METHYL ISOCYANIDE 1-([ISOCYANO(PHENYL)METHYL]SULPHONYL)-4-METHYLBENZENE alfa-Tosylbenzylisocyanide 1-(isocyano(p-tolyl)methylsulfonyl)-4-methylbenzene Isocyano(phenyl)methyl 4-methylphenyl sulphone Benzene,1-[(isocyanophenylMethyl)sulfonyl]-4-Methyl- alpha-(Toluene-4-sulphonyl)benzyl isocyanide a-(4-Tolylsulfonyl)benzylisocyanide alpha-(Toluene-4-sulphonyl)benzyl isocyanide, 4-{[Isocyano(phenyl)methyl]sulphonyl}toluene, alpha-Tosylbenzyl isocyanide Isocyano(phenyl)methyl 4-methylphenyl sulphone 97% 1-(Isocyano-phenyl-Methanesulfonyl)-4-Methyl-benzene 1-((Isocyano(phenyl)methyl)sulfonyl)-4-methylbenzene Isocyano(phenyl)methyl4-methylphenylsulphone97% -(p-Toluenesulfonyl)benzyl Isocyanide α-(p-Toluenesulfonyl)benzyl Isocyanide alpha-(p-Toluenesulfonyl)benzyl Isocyanide 5-(isocyanomethylsulfonyl)-2-methyl-5-phenylcyclohexa-1,3-diene Isocyano(phenyl)methyl 4-methylphenyl sulfone SKL019 α-(p-Toluenesulfonyl)benzyl Isocyanide 36635-66-2 C15H13NO2S pharmacetical