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CAS

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23074-07-9

3-hydroxyglibenclamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23074-07-9 Structure

  • Basic information

    1. Product Name: 3-hydroxyglibenclamide
    2. Synonyms: 3-hydroxyglibenclamide
    3. CAS NO:23074-07-9
    4. Molecular Formula: C23H28ClN3O6S
    5. Molecular Weight: 510.00292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23074-07-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 1.41g/cm3
    6. Refractive Index: 1.63
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-hydroxyglibenclamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-hydroxyglibenclamide(23074-07-9)
    11. EPA Substance Registry System: 3-hydroxyglibenclamide(23074-07-9)

  • 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: 23074-07-9(Hazardous Substances Data)

23074-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23074-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23074-07:
(7*2)+(6*3)+(5*0)+(4*7)+(3*4)+(2*0)+(1*7)=79
79 % 10 = 9
So 23074-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H28ClN3O6S/c1-33-21-10-7-16(24)13-20(21)22(29)25-12-11-15-5-8-19(9-6-15)34(31,32)27-23(30)26-17-3-2-4-18(28)14-17/h5-10,13,17-18,28H,2-4,11-12,14H2,1H3,(H,25,29)(H2,26,27,30)

23074-07-9Downstream Products

23074-07-9Relevant articles and documents

Hydroxyl-Substituted sulfonylureas as potent inhibitors of specific [3H]Glyburide binding to rat brain synaptosomes

Hill, Ronald A.,Rudra, Sonali,Peng, Bo,Roane, David S.,Bounds, Jeffrey K.,Zhang, Yang,Adloo, Ahmad,Lu, Tiansheng

, p. 2099 - 2113 (2003)

We are seeking to discover potent CNS-active sulfonylureas with structural features that allow for the formation of several types of prodrugs. We report herein the syntheses of compounds comprising an initial series of hydroxyl-substituted analogues of the potent ATP-sensitive potassium channel blockers glyburide (glibenclamide) and gliquidone. Somewhat unexpectedly, several of the compounds were found to be comparably potent to glyburide as inhibitors of specific [3H]glyburide binding in rat brain preparations.

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