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83020-32-0

N-Phenyl-benzimidic acid (S)-2-cyano-1,2,2-trimethyl-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83020-32-0 Structure

  • Basic information

    1. Product Name: N-Phenyl-benzimidic acid (S)-2-cyano-1,2,2-trimethyl-ethyl ester
    2. Synonyms:
    3. CAS NO:83020-32-0
    4. Molecular Formula:
    5. Molecular Weight: 292.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83020-32-0.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: N-Phenyl-benzimidic acid (S)-2-cyano-1,2,2-trimethyl-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Phenyl-benzimidic acid (S)-2-cyano-1,2,2-trimethyl-ethyl ester(83020-32-0)
    11. EPA Substance Registry System: N-Phenyl-benzimidic acid (S)-2-cyano-1,2,2-trimethyl-ethyl ester(83020-32-0)

  • 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: 83020-32-0(Hazardous Substances Data)

83020-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83020-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,2 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83020-32:
(7*8)+(6*3)+(5*0)+(4*2)+(3*0)+(2*3)+(1*2)=90
90 % 10 = 0
So 83020-32-0 is a valid CAS Registry Number.

83020-32-0Downstream Products

83020-32-0Relevant articles and documents

PHOTOINDUCED CYCLOADDITIONS OF ELECTRON DEFICIENT NITRONES TO ALKENES

Griffin, G. W.,Lankin, D. C.,Bhacca, N. S.,Terasawa, H.,Sehgal, R. K.

, p. 2753 - 2756 (1982)

Oxaziridines are proposed as intermediates in the photoinduced cycloadditions of electron deficient nitrones to dipolarophiles.

Novel Photocycloadditions of Electron-Deficient Nitrones to 2-Methyl-2-butene

Sehgal, R. K.,Griffin, G. W.

, p. 513 - 517 (2007/10/02)

In order to decrease the ground state reactivity and increase their potential for cycloadditions, cyano- and methoxycarbonyl-substituted nitrones 1a and 1b, respectively, were prepared and irradiated in the presence of electron-rich alkenes such as 2 to afford the corresponding oxazolidines in which the oxygen atom becomes attached to the least substituted terminus of the olefin and nitrogen attaches the more highly substituted counterpart.While the oxazolidines 12a and 12b obtained from 1b, via the intermediacy of oxaziridine(s) 15 and subsequent N-O bond scission, are isolated and characterized, the oxazolidine(s) 18 formed by cycl ization of 1a are more labile and may undergo ionization to the stabilized oxazolinium ion 19 followed by nucleophilic attack by cyanide ion with accompanying ring opening to afford 6.A sequential diradical mechanism is proposed to rationalize the formation of the observed photoproducts 5 and 6.

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