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1-phenyl-3-propyl-1H-pyrrole-2,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 75066-67-0 Structure
  • Basic information

    1. Product Name: 1-phenyl-3-propyl-1H-pyrrole-2,5-dione
    2. Synonyms: 1-phenyl-3-propyl-1H-pyrrole-2,5-dione
    3. CAS NO:75066-67-0
    4. Molecular Formula:
    5. Molecular Weight: 215.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 75066-67-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-phenyl-3-propyl-1H-pyrrole-2,5-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-3-propyl-1H-pyrrole-2,5-dione(75066-67-0)
    11. EPA Substance Registry System: 1-phenyl-3-propyl-1H-pyrrole-2,5-dione(75066-67-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 75066-67-0(Hazardous Substances Data)

75066-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75066-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,6 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75066-67:
(7*7)+(6*5)+(5*0)+(4*6)+(3*6)+(2*6)+(1*7)=140
140 % 10 = 0
So 75066-67-0 is a valid CAS Registry Number.

75066-67-0Downstream Products

75066-67-0Relevant articles and documents

Palladium-Catalyzed Carbonylative Cyclization of Terminal Alkynes and Anilines to 3-Substituted Maleimides

Xu, Jian-Xing,Wu, Xiao-Feng

, p. 3376 - 3380 (2018)

Herein, we describe an interesting palladium-catalyzed protocol for the carbonylative synthesis of 3-substituted maleimides. By annulation of simple anilines with terminal alkynes under carbon monoxide pressure, the desired 3-substituted maleimides can be

Cumulated Ylides, XVII. Synthesis of Cyclic Compounds from Triphenylphosphorane and Oxocarboxylic Acids - A Novel Method for Anellation

Bestmann, Hans Juergen,Schade, Gerold,Luetke, Harry,Moenius, Thomas

, p. 2640 - 2658 (2007/10/02)

By entropically supported intramolecular Wittig reaction from α-keto carboxylic acids 23 with triphenylphosphorane (1) N-phenylmaleinisoimides 26 and -imides 29 are formed.The compounds 26 can be rearranged into 29 with a catalytic amount of sodium azide. - From γ-keto carboxylic acids 30 3-substituted 2-cyclopenten-1-ones 37 can be derived via the 3,6-dioxo-2-(triphenylphosphoranylidene)alkananilides 33.Analogously, 3-substituted 2-cyclohexen-1-ones 49 are formed from δ-keto carboxylic acids 46. o-Acylbenzoic acids 38, in the case R = H, are converted with 1 into the benzazepinedione derivative 44, and in the case R unlike H into 3-substituted 1-oxo-1H-indene-2-carboxanilides 45. - Starting from oxo carboxylic acids, possessing the carbonyl function in a ring, five- and six-membered rings can be anellated in a simple way.

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