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23141-82-4

3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23141-82-4 Structure

  • Basic information

    1. Product Name: 3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
    2. Synonyms: 3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide
    3. CAS NO:23141-82-4
    4. Molecular Formula:
    5. Molecular Weight: 263.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23141-82-4.mol

  • Chemical Properties

    1. Melting Point: 208-210 °C
    2. Boiling Point: 570.2±60.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.606±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide(23141-82-4)
    11. EPA Substance Registry System: 3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide(23141-82-4)

  • 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: 23141-82-4(Hazardous Substances Data)

23141-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23141-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23141-82:
(7*2)+(6*3)+(5*1)+(4*4)+(3*1)+(2*8)+(1*2)=74
74 % 10 = 4
So 23141-82-4 is a valid CAS Registry Number.

23141-82-4Downstream Products

23141-82-4Relevant articles and documents

Photolytic decomposition of hydrochlorothiazide

Tamat,Moore

, p. 180 - 183 (2007/10/02)

Hydrochlorothiazide decomposes upon irradiation with near-UV light (λ > 310 nm) both in methanol and aqueous solutions. In the photolysis the chlorine substituent is removed to be replaced by either -H or -OR from the solvent ROH. Hydrolysis of the thiadiazine ring is superimposed upon the dechlorination. The presence of oxygen inhibits the decomposition. The mechanism of the photolysis is suggested to involve cation radical formation which facilitates the hydrolysis step. 5-Chloro-2,4-disulphonamido-aniline, the normal hydrolysis product from hydrochlorothiazide, is also susceptible to photolytic dechlorination by a similar mechanism.

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