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I-PROPYLISOCYANIDE

CAS No.
598-45-8
Chemical Name:
I-PROPYLISOCYANIDE
Synonyms
2-isocyanopropane;1-Propylisocyanide;I-PROPYLISOCYANIDE;2-Isocyano-propane;2-Isonitrilopropane;ISOPROPYLISOCYANIDE;Isopropyl-isonitrile;isopropylcarbylamine;i-Propylisocyanide,99%;Isopropyl isocyanide 97%
CBNumber:
CB0182698
Molecular Formula:
C4H7N
Molecular Weight:
69.11
MDL Number:
MFCD00015503
MOL File:
598-45-8.mol
MSDS File:
SDS
Last updated:2023-04-23 13:52:06

I-PROPYLISOCYANIDE Properties

Boiling point 75 °C(lit.)
Density 0.733 g/mL at 25 °C(lit.)
refractive index n20/D 1.371(lit.)
Flash point 69 °F
storage temp. 2-8°C
form liquid
color colorless
Specific Gravity 0.7596
Stability store cold

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS06
Signal word  Danger
Hazard statements  H225-H301+H311+H331
Precautionary statements  P210-P233-P280-P301+P310-P303+P361+P353-P304+P340+P311
Hazard Codes  F,T
Risk Statements  11-23/24/25
Safety Statements  16-23-26-33-36/37/39-45
RIDADR  UN 1992 3/PG 2
WGK Germany  3

I-PROPYLISOCYANIDE price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 553344 Isopropyl isocyanide 97% 598-45-8 500mg $103.2 2024-03-01 Buy
Strem Chemicals 06-1850 i-Propylisocyanide, min. 97% 598-45-8 1g $328 2024-03-01 Buy
Strem Chemicals 06-1850 i-Propylisocyanide, min. 97% 598-45-8 5g $1308 2024-03-01 Buy
American Custom Chemicals Corporation CHM0117010 ISOPROPYL ISOCYANIDE 95.00% 598-45-8 500MG $586.49 2021-12-16 Buy
Product number Packaging Price Buy
553344 500mg $103.2 Buy
06-1850 1g $328 Buy
06-1850 5g $1308 Buy
CHM0117010 500MG $586.49 Buy

I-PROPYLISOCYANIDE Chemical Properties,Uses,Production

Uses

Isopropyl isocyanide may be used in the preparation of:

  • Ugi ligand A2C11I1, which is employed in the solid-phase Ugi synthesis.
  • Pentafluorophenyl (PFP) functional monomers, via Passerini reaction.
  • Dinuclear copper complex [Cu2(μ-PiPr2bipy)2{μ-CNCH(CH3)2}](PF6)2 [PiPr2bipy = 6-(diisopropylphosphanyl)-2,2′-bipyridine].
  • (3E)-(Imino)thiaisoindoline 1,1-dioxide derivative.
  • N,N′-diisopropylcarbodiimide (DIC) analog via reaction with propan-2-amine.
  • 1-t-butyl-2-isopropyldiaziridinone via reaction with 2-methyl-2-nitrosopropane
  • isopropyl isocyanate via reaction with ozone
  • 1-phthalimidoazetidines via [1+3]cycloaddition reaction with 1-pththalimidoaziridines

Preparation

To a flask containing 100 ml (0.85 mole) of distilled quinoline is added with stirring 41 gm (0.214 mole) of /7-toluenesulfonyl chloride (see Note), and the solution is warmed to 75°C. Then 18.4 gm (0.212 mole) of isopropylformamide is added and the pressure of the system is reduced to 70 mm Hg. The isopropylisonitrile as it forms distills into a liquid nitrogencooled receiver. (Dry ice is not as effective but may be used.) The product is redistilled to afford 4.2 gm (30%), b.p. 88-89°C (735 mm Hg).
Preparation of Isopropyl Isonitrile

General Description

Isopropyl isocyanide is an alkyl isocyanide.

I-PROPYLISOCYANIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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I-PROPYLISOCYANIDE Spectrum

ISOPROPYLISOCYANIDE I-PROPYLISOCYANIDE 2-isocyanopropane 2-Isocyano-propane 2-Isonitrilopropane Isopropyl-isonitrile 1-Propylisocyanide i-Propylisocyanide,99% isopropylcarbylamine 1-Methyl-1-isocyanoethane i-Propylisocyanide, min. 97% Isopropyl isocyanide 97% I-PROPYLISOCYANIDE,MIN.97% 598-45-8 CH32CHNC iC3H7NC Organic Building Blocks Nitrogen Compounds Isocyanides Building Blocks organic compound Isocyanides Nitrogen Compounds Organic Building Blocks