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CAS

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86212-33-1

4,5-di(p-chlorophenyl)imidazoline-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86212-33-1 Structure

  • Basic information

    1. Product Name: 4,5-di(p-chlorophenyl)imidazoline-2-thione
    2. Synonyms: 4,5-di(p-chlorophenyl)imidazoline-2-thione
    3. CAS NO:86212-33-1
    4. Molecular Formula:
    5. Molecular Weight: 323.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86212-33-1.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: 4,5-di(p-chlorophenyl)imidazoline-2-thione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,5-di(p-chlorophenyl)imidazoline-2-thione(86212-33-1)
    11. EPA Substance Registry System: 4,5-di(p-chlorophenyl)imidazoline-2-thione(86212-33-1)

  • 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: 86212-33-1(Hazardous Substances Data)

86212-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86212-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86212-33:
(7*8)+(6*6)+(5*2)+(4*1)+(3*2)+(2*3)+(1*3)=121
121 % 10 = 1
So 86212-33-1 is a valid CAS Registry Number.

86212-33-1Relevant articles and documents

REACTIONS WITH 4,5-DI(p-CHLOROPHENYL)IMIDAZOLIDINE-2-THIONE

Sharaf, Mohie A. F.,Ezat, El-Emam H. M.,Hammouda, Hamdy A. A.

, p. 19 - 28 (2007/10/02)

Alkylation of 1 gave the S-alkyl derivatives 3a-c. The S-methyl derivative 3a reacted with amines, with the elimination of methanethiol, to give the 2-amino derivatives 4a-c; with thiosemicarbazide to yield the imidazos-triazole 6; and with anthranilic acids to yield the imidazoquinazolines 8a,b. Compound 3a reacted also with active-methylene compounds to give the ketene aminals 10a-c. Alkylation of 1 with dihaloalkanes afforded the bis compounds 14a,b. In the case of 1,2-dibromoethane, the imidazothiazole 13 was obtained. The reaction of 1 with α-halo-ketones led directly to the imidazothiazoles 15a-c and 17. However, with halo-acetoacetanilides, the acyclic intermediates 20d-g were isolated. Key words: Alkylation, ketene aminals, imidazo heterocycles.

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