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13232-81-0

10-iodo-5,10-dihydrophenarsazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13232-81-0 Structure

  • Basic information

    1. Product Name: 10-iodo-5,10-dihydrophenarsazine
    2. Synonyms: 10-iodo-5,10-dihydrophenarsazine
    3. CAS NO:13232-81-0
    4. Molecular Formula:
    5. Molecular Weight: 369.036
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13232-81-0.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: 10-iodo-5,10-dihydrophenarsazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-iodo-5,10-dihydrophenarsazine(13232-81-0)
    11. EPA Substance Registry System: 10-iodo-5,10-dihydrophenarsazine(13232-81-0)

  • 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: 13232-81-0(Hazardous Substances Data)

13232-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13232-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13232-81:
(7*1)+(6*3)+(5*2)+(4*3)+(3*2)+(2*8)+(1*1)=70
70 % 10 = 0
So 13232-81-0 is a valid CAS Registry Number.

13232-81-0Downstream Products

13232-81-0Relevant articles and documents

Reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid

Gavrilov,Karavanov,Musin,Garieva,Musin

, p. 1212 - 1215 (2004)

We have studied the reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid and we have established the structure of the products by high-resolution mass spectrometry. We have shown that when the methyl group is replaced by a phenyl group in 5,10-dihydrophenarsazine 10-oxides, cleavage of the endocyclic arsenic-carbon bonds occurs. 2004 Springer Science+Business Media, Inc.

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