I-PROPYLISOCYANIDE

I-PROPYLISOCYANIDE
  • CAS No.:598-45-8

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
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I-PROPYLISOCYANIDE Basic information
Product Name:I-PROPYLISOCYANIDE
Synonyms:ISOPROPYLISOCYANIDE;I-PROPYLISOCYANIDE;2-isocyanopropane;2-Isocyano-propane;2-Isonitrilopropane;Isopropyl-isonitrile;1-Propylisocyanide;i-Propylisocyanide,99%
CAS:598-45-8
MF:C4H7N
MW:69.11
EINECS:
Product Categories:organic compound;Isocyanides;Nitrogen Compounds;Organic Building Blocks
Mol File:598-45-8.mol
I-PROPYLISOCYANIDE Chemical Properties
Boiling point 75 °C(lit.)
density 0.733 g/mL at 25 °C(lit.)
refractive index n20/D 1.371(lit.)
Fp 69 °F
storage temp. 2-8°C
form liquid
Specific Gravity0.7596
color colorless
Stability:store cold
Safety Information
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
MSDS Information
ProviderLanguage
SigmaAldrich English
I-PROPYLISOCYANIDE Usage And Synthesis
UsesIsopropyl 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
PreparationTo 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).
General DescriptionIsopropyl isocyanide is an alkyl isocyanide.
I-PROPYLISOCYANIDE Preparation Products And Raw materials
Raw materialsisopropyl isocyanide dichloride

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