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3-(p-tolylthio)succinic anhydride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91344-83-1 Structure
  • Basic information

    1. Product Name: 3-(p-tolylthio)succinic anhydride
    2. Synonyms: 3-(p-tolylthio)succinic anhydride
    3. CAS NO:91344-83-1
    4. Molecular Formula:
    5. Molecular Weight: 222.265
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91344-83-1.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: 3-(p-tolylthio)succinic anhydride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(p-tolylthio)succinic anhydride(91344-83-1)
    11. EPA Substance Registry System: 3-(p-tolylthio)succinic anhydride(91344-83-1)
  • 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: 91344-83-1(Hazardous Substances Data)

91344-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91344-83-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91344-83:
(7*9)+(6*1)+(5*3)+(4*4)+(3*4)+(2*8)+(1*3)=131
131 % 10 = 1
So 91344-83-1 is a valid CAS Registry Number.

91344-83-1Relevant articles and documents

Mechanistic Investigation of Castagnoli-Cushman Multicomponent Reactions Leading to a Three-Component Synthesis of Dihydroisoquinolones

Howard, Sara Y.,Di Maso, Michael J.,Shimabukuro, Kristin,Burlow, Noah P.,Tan, Darlene Q.,Fettinger, James C.,Malig, Thomas C.,Hein, Jason E.,Shaw, Jared T.

, p. 11599 - 11607 (2021)

The mechanisms for the three- and four-component variants of the Castagnoli-Cushman reaction (CCR) have been investigated. A series of crossover experiments were conducted to probe the structure and reactivity of known amide-acid intermediates for the thr

Antimicrobial composition and method containing N-(3,5-dihalophenyl)-imide compounds

-

, (2008/06/13)

Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula, STR1 wherein X and X' each represent halogens and A represents a substituted ethylene such as chloroethylene, C1 - C4 alkylthioethylene, C1 - C2 alkyl-ethylene or 1,2-di-C1 - C2 -alkyl-ethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene. The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N-(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.

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