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2-methylseleno-5-p-chlorophenylmethylene-thiazolinone-4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79851-82-4 Structure
  • Basic information

    1. Product Name: 2-methylseleno-5-p-chlorophenylmethylene-thiazolinone-4
    2. Synonyms:
    3. CAS NO:79851-82-4
    4. Molecular Formula:
    5. Molecular Weight: 316.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79851-82-4.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-methylseleno-5-p-chlorophenylmethylene-thiazolinone-4(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methylseleno-5-p-chlorophenylmethylene-thiazolinone-4(79851-82-4)
    11. EPA Substance Registry System: 2-methylseleno-5-p-chlorophenylmethylene-thiazolinone-4(79851-82-4)
  • 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: 79851-82-4(Hazardous Substances Data)

79851-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79851-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,5 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79851-82:
(7*7)+(6*9)+(5*8)+(4*5)+(3*1)+(2*8)+(1*2)=184
184 % 10 = 4
So 79851-82-4 is a valid CAS Registry Number.

79851-82-4Downstream Products

79851-82-4Relevant articles and documents

INTRODUCTION OF SELENIUM TO HETEROCYCLIC COMPOUNDS. PART II. SYNTHESIS OF 3-ALKYL-2-SELENOHYDANTOINS, 2-SELENOHYDANTOIN-3-ACETIC ACID AND 2-SELENORHODANINES WITH DOUBLE BOND AT C-5

Korohoda, Maria Jolanta

, p. 359 - 369 (2007/10/02)

The earlier described method was applied to synthesize so far unknown benzylidene derivatives of 3-methyl-2-selenohydantoin, 2-selenohydantoin-3-acetic acid and 2-selenorhodanine.The structures of these compounds were confirmed by the spectral data.Some p

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