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21406-30-4

Carbamodithioic acid, benzoyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21406-30-4 Structure

  • Basic information

    1. Product Name: Carbamodithioic acid, benzoyl-, methyl ester
    2. Synonyms:
    3. CAS NO:21406-30-4
    4. Molecular Formula: C9H9NOS2
    5. Molecular Weight: 211.309
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21406-30-4.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: Carbamodithioic acid, benzoyl-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamodithioic acid, benzoyl-, methyl ester(21406-30-4)
    11. EPA Substance Registry System: Carbamodithioic acid, benzoyl-, methyl ester(21406-30-4)

  • 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: 21406-30-4(Hazardous Substances Data)

21406-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21406-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21406-30:
(7*2)+(6*1)+(5*4)+(4*0)+(3*6)+(2*3)+(1*0)=64
64 % 10 = 4
So 21406-30-4 is a valid CAS Registry Number.

21406-30-4Relevant articles and documents

An α-hydrazinoalkylphosphonate as building block for novel N-phosphonoalkylheterocycles

Li, Zai-Guo,Sun, Hui-Kai,Wang, Qing-Min,Huang, Run-Qiu

, p. 384 - 386 (2003)

α-Hydrazinoalkylphosphonate 3 is a useful building block for the syntheses of novel N-phosphonoalkylheterocycles. N-phosphonoalkylpyrazoles 8 and 9 were prepared by the cyclization reaction of 3 with malfunctioned ethenes 5 and 6 in ethanol under reflux. N-Phosphonoalkyltriazole 10 was synthesized from 3 with N-dimethylthiomethylene benzoyl amide 4 in ethanol under reflux. The structures were confirmed by IR, 1H NMR, mass spectroscopy, and elemental analysis. At the same time, the preparation of 4 was investigated.

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