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89332-92-3

2-Furancarbothioamide, N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89332-92-3 Structure

  • Basic information

    1. Product Name: 2-Furancarbothioamide, N-methyl-
    2. Synonyms: 2-Furancarbothioamide,N-methyl;N-methyl-2-thiofuramide;N-methyl 2-furanecarbothioamide;furan-2-carbothioic acid methylamide;Furan-2-thiocarbonsaeure-methylamid;
    3. CAS NO:89332-92-3
    4. Molecular Formula: C6H7NOS
    5. Molecular Weight: 141.194
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89332-92-3.mol

  • Chemical Properties

    1. Melting Point: 71-71.5 °C(Solv: ligroine (8032-32-4))
    2. Boiling Point: 195.1±32.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.172±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Furancarbothioamide, N-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Furancarbothioamide, N-methyl-(89332-92-3)
    11. EPA Substance Registry System: 2-Furancarbothioamide, N-methyl-(89332-92-3)

  • 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: 89332-92-3(Hazardous Substances Data)

89332-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89332-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89332-92:
(7*8)+(6*9)+(5*3)+(4*3)+(3*2)+(2*9)+(1*2)=163
163 % 10 = 3
So 89332-92-3 is a valid CAS Registry Number.

89332-92-3Downstream Products

89332-92-3Relevant articles and documents

SOME NOVEL ASPECTS OF REGIOSELECTIVITY IN 1,3 DIPOLAR CYCLOADDITIONS OF 4H-1-BENZOPYRAN-4-THIONE

Baruah, Arpan K.,Prajapati, Dipak,Sandhu, Jagir S.

, p. 6137 - 6142 (1988)

4H-1-Benzopyran-4-thione (1) reacted smoothly with nitrilimines (3a-e) to afford regioselective cycloadducts (4a-e) in good yields.In contrast,benzonitrile oxide (6) and aldonitrones (7a-d) reacted preferentially at the thione function.The unstable cycloadduct (8) or (9) ruptured to give as isolable products chromone (10) and phenyl isothiocyanate (11) and the thioamides (12a-d).This indirectly proves the site of attack of the dipole at the thione group.

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