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1428555-12-7

C20H22BrF3N2O5S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428555-12-7 Structure

  • Basic information

    1. Product Name: C20H22BrF3N2O5S
    2. Synonyms: C20H22BrF3N2O5S
    3. CAS NO:1428555-12-7
    4. Molecular Formula:
    5. Molecular Weight: 539.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428555-12-7.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: C20H22BrF3N2O5S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H22BrF3N2O5S(1428555-12-7)
    11. EPA Substance Registry System: C20H22BrF3N2O5S(1428555-12-7)

  • 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: 1428555-12-7(Hazardous Substances Data)

1428555-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428555-12-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,5,5 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1428555-12:
(9*1)+(8*4)+(7*2)+(6*8)+(5*5)+(4*5)+(3*5)+(2*1)+(1*2)=167
167 % 10 = 7
So 1428555-12-7 is a valid CAS Registry Number.

1428555-12-7Downstream Products

1428555-12-7Relevant articles and documents

Deconstruction of sulfonamide inhibitors of the urotensin receptor (UT) and design and synthesis of benzylamine and benzylsulfone antagonists

Taylor, Steven J.,Soleymanzadeh, Fariba,Muegge, Ingo,Akiba, Isamu,Taki, Naoyuki,Ueda, Saisoku,Mainolfi, Elizabeth,Eldrup, Anne B.

supporting information, p. 2177 - 2180 (2013/04/24)

Potent small molecule antagonists of the urotensin receptor are described. These inhibitors were derived via systematically deconstructing a literature inhibitor to understand the basic pharmacophore and key molecular features required to inhibit the prot

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