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2,4-dihydroxyphenylthiolanium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33127-94-5 Structure
  • Basic information

    1. Product Name: 2,4-dihydroxyphenylthiolanium chloride
    2. Synonyms: 2,4-dihydroxyphenylthiolanium chloride
    3. CAS NO:33127-94-5
    4. Molecular Formula:
    5. Molecular Weight: 232.731
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33127-94-5.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: 2,4-dihydroxyphenylthiolanium chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dihydroxyphenylthiolanium chloride(33127-94-5)
    11. EPA Substance Registry System: 2,4-dihydroxyphenylthiolanium chloride(33127-94-5)
  • 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: 33127-94-5(Hazardous Substances Data)

33127-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33127-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,2 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33127-94:
(7*3)+(6*3)+(5*1)+(4*2)+(3*7)+(2*9)+(1*4)=95
95 % 10 = 5
So 33127-94-5 is a valid CAS Registry Number.

33127-94-5Relevant articles and documents

SYNTHESIS OF SULFONIUM CHLORIDES FROM THIOPHANE, PHENOLS, AND CHLORINE

Sakharova, S. N.,Karaulova, E. N.,Krapivin, A. M.,Gal'pern, G. D.

, p. 1513 - 1516 (2007/10/02)

A one-stage synthesis was realized for 2(3)-methyl-4-hydroxy-, 2,4-dihydroxy-, 2,3,4-trihydroxy-, and 2,5-dihydroxyphenylthiophanium chlorides by the reactions of substituted phenols with thiophane and chlorine.The yields (57-75percent) of the products varied in line with the activity of the phenols.

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