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1259931-96-8

C36H37F2N7O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1259931-96-8 Structure

  • Basic information

    1. Product Name: C36H37F2N7O3S
    2. Synonyms:
    3. CAS NO:1259931-96-8
    4. Molecular Formula:
    5. Molecular Weight: 685.798
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1259931-96-8.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: C36H37F2N7O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H37F2N7O3S(1259931-96-8)
    11. EPA Substance Registry System: C36H37F2N7O3S(1259931-96-8)

  • 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: 1259931-96-8(Hazardous Substances Data)

1259931-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1259931-96-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,9,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1259931-96:
(9*1)+(8*2)+(7*5)+(6*9)+(5*9)+(4*3)+(3*1)+(2*9)+(1*6)=198
198 % 10 = 8
So 1259931-96-8 is a valid CAS Registry Number.

1259931-96-8Downstream Products

1259931-96-8Relevant articles and documents

Discovery of N-benzyl-N′-(4-pipyridinyl)urea CCR5 antagonists as anti-HIV-1 agents (II): Modification of the acyl portion

Duan, Maosheng,Peckham, Jennifer,Edelstein, Mark,Ferris, Robert,Kazmierski, Wieslaw M.,Spaltenstein, Andrew,Wheelan, Pat,Xiong, Zhiping

scheme or table, p. 7401 - 7404 (2011/02/22)

Modification of the acyl moiety in the CCR5 lead molecule 2 led to identification of several new classes of CCR5 antagonists. Antiviral activity and pharmacokinetic properties of the synthesized compounds were evaluated. Structure-activity relationship (S

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