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6,8-dibromo-7-hydroxyisoflavone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19816-36-5 Structure
  • Basic information

    1. Product Name: 6,8-dibromo-7-hydroxyisoflavone
    2. Synonyms: 6,8-dibromo-7-hydroxyisoflavone
    3. CAS NO:19816-36-5
    4. Molecular Formula:
    5. Molecular Weight: 396.035
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19816-36-5.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: 6,8-dibromo-7-hydroxyisoflavone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,8-dibromo-7-hydroxyisoflavone(19816-36-5)
    11. EPA Substance Registry System: 6,8-dibromo-7-hydroxyisoflavone(19816-36-5)
  • 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: 19816-36-5(Hazardous Substances Data)

19816-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19816-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19816-36:
(7*1)+(6*9)+(5*8)+(4*1)+(3*6)+(2*3)+(1*6)=135
135 % 10 = 5
So 19816-36-5 is a valid CAS Registry Number.

19816-36-5Upstream product

19816-36-5Relevant articles and documents

Tritium Labeling of 7-Isopropoxyisoflavone

Oetvoes, Ferenc,Toth, Geza,Szatmari, Istvan,Levai, Ferenc

, p. 497 - 504 (2007/10/03)

Catalytic tritiodehalogenation of 8-bromoipriflavone and 6,8-dibromoipriflavone resulted in [8-3H]ipriflavone (3) and [6,8-3H2]ipriflavone (7) with specific activities of 1.08 TBq/mmol (29.2 Ci/mmol) and 1.94 TBq/mmol (52.4 Ci/mmol), respectively. 8-Bromoipriflavone was synthesized by direct bromination of ipriflavone, while 6,8-dibromoipriflavone was formed by isopropylation of the phenolic OH group of 6,8-dibromo-7-hydroxyisoflavone which itself was prepared from 7-hydroxyisoflavone and elemental bromine.

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