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4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide

    Cas No: 95707-55-4

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  • 95707-55-4 Structure
  • Basic information

    1. Product Name: 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide
    2. Synonyms: 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide
    3. CAS NO:95707-55-4
    4. Molecular Formula:
    5. Molecular Weight: 292.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95707-55-4.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: 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide(95707-55-4)
    11. EPA Substance Registry System: 4-(3-hydroxy-3-phenyltriaz-1-en-1-yl)benzenesulfonamide(95707-55-4)
  • 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: 95707-55-4(Hazardous Substances Data)

95707-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95707-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,0 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95707-55:
(7*9)+(6*5)+(5*7)+(4*0)+(3*7)+(2*5)+(1*5)=164
164 % 10 = 4
So 95707-55-4 is a valid CAS Registry Number.

95707-55-4Relevant articles and documents

Synthesis of sulpha drug based hydroxytriazene derivatives: Anti-diabetic, antioxidant, anti-inflammatory activity and their molecular docking studies

Baroliya, Prabhat K.,Chauhan, R. S.,Dayma, Varsha,Dwivedi, Aparna,Goswami, A. K.,Sharma, Poonam,Tripathi, I. P.,Vanangamudi, Murugesan

, (2020)

Herein, we report synthesis, characterization, anti-diabetic, anti-inflammatory and anti-oxidant activities of hydroxytriazenes derived from sulpha drugs, namely sulphanilamide, sulphadiazine, sulphapyridine and sulphamethazine. Before biological screening of the compounds, theoretical prediction using PASS was done which indicates probable activities ranging from Pa (probable activity) values 65–98% for anti-inflammatory activity. As per the predication, experimental validation of some of the predicted activities particularly anti-diabetic, anti-inflammatory and anti-oxidant was done. Anti-diabetic activities have been screened using two methods namely α-amylase and α-glucosidase inhibition method and IC50 values were ranging from 66 to 260 and 148 to 401 μg/mL, while for standard drug acarbose the values were 12 μg/mL and 70 μg/mL, respectively. Docking studies have also been done for antidiabetic target pancreatic alpha amylase. The molecular docking studies in α-amylase enzyme reveal that the middle phenyl ring of all the compounds mainly occupies in the small hydrophobic pocket formed by the Ala198, Trp58, Leu162, Leu165 and Ile235 residues and sulphonamide moiety establish H-bond interaction by two water molecules. Further, anti-inflammatory activity has been evaluated using carrageenan induced paw-edema method and results indicate excellent anti-inflammatory activity by hydroxytriazenes (71 to 97%) and standard drug diclofenac 94% after 4 h of treatment. Moreover, antioxidant effect of the compounds was tested using DPPH and ABTS methods. All the compounds displayed good results (24–488 μg/mL) against ABTS radical and many compounds are more active than ascorbic acid (69 μg/mL) while all other compounds showed moderate activity against DPPH radical (292–774 μg/mL) and ascorbic acid (29 μg/mL). Thus, the studies reveal potential of sulfa drug based hydroxytriazenes as candidates for antidiabetic, anti-inflammatory and antioxidant activities which have been experimentally validated.

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