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CAS

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80232-92-4

2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80232-92-4 Structure

  • Basic information

    1. Product Name: 2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole
    2. Synonyms: 2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole
    3. CAS NO:80232-92-4
    4. Molecular Formula:
    5. Molecular Weight: 294.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80232-92-4.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: 2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole(80232-92-4)
    11. EPA Substance Registry System: 2-phenylimino-3-phenyl-4-isopropyl-2,3-dihydrothiazole(80232-92-4)

  • 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: 80232-92-4(Hazardous Substances Data)

80232-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80232-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80232-92:
(7*8)+(6*0)+(5*2)+(4*3)+(3*2)+(2*9)+(1*2)=104
104 % 10 = 4
So 80232-92-4 is a valid CAS Registry Number.

80232-92-4Downstream Products

80232-92-4Relevant articles and documents

SYNTHETIC APPLICATIONS OF 2-CHLOROOXIRANES: PREPARATION OF THIAZOLES, DIHYDROTHIAZOLES AND SELENAZOLES

Gasteiger, Johann,Herzig, Christian

, p. 2607 - 2611 (1981)

The reaction of 2-chlorooxiranes 1 with thioamides and thioureas provides access to thiazoles, 4-hydroxy-4,5-dihydrothiazoles and 2-imino-2,3-dihydrothiazoles under mild conditions and excellent yields.With 1 and selenourea, near quantitative yields of se

Synthesis and Mercuration of Some New 3-Aryl-2-arylimino-4,5-disubstituted-δ4-thiazolines and Their Fungicidal and Bactericidal Activities

Mohanty, J.,Mahapatra, G. N.

, p. 52 - 55 (2007/10/02)

A series of new 3-aryl-2-arylimino-4,5-disubstituted-Δ4-thiazolines (I) have been synthesised by condensing various ketones having active methylene group with sym-diarylthioureas in the presence of bromine.The thiazolines (I) on mercuration with one equivalent of mercuric acetate in acetic acid give 3-(acetoxymercuriaryl)-2-arylimino-4,5-disubstituted-Δ4-thiazolines (II).All the compounds have been assayed against the fungus Pyricularia oryzae (Cav) and the bacteria Esch. coli and Staph. aureus, and the structure-activity relationship has been discussed.

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