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1173898-59-3

C36H44F4N4O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1173898-59-3 Structure

  • Basic information

    1. Product Name: C36H44F4N4O3
    2. Synonyms:
    3. CAS NO:1173898-59-3
    4. Molecular Formula:
    5. Molecular Weight: 656.764
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1173898-59-3.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: C36H44F4N4O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C36H44F4N4O3(1173898-59-3)
    11. EPA Substance Registry System: C36H44F4N4O3(1173898-59-3)

  • 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: 1173898-59-3(Hazardous Substances Data)

1173898-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173898-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,8,9 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1173898-59:
(9*1)+(8*1)+(7*7)+(6*3)+(5*8)+(4*9)+(3*8)+(2*5)+(1*9)=203
203 % 10 = 3
So 1173898-59-3 is a valid CAS Registry Number.

1173898-59-3Upstream product

1173898-59-3Downstream Products

1173898-59-3Relevant articles and documents

Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 2: Discovery of highly potent anti-HIV agents

Li, Ben,Jones, Eric Dale,Zhou, Enkun,Chen, Li,Baylis, Dean Cameron,Yu, Shanghai,Wang, Miao,He, Xing,Coates, Jonathan Alan Victor,Rhodes, David Ian,Pei, Gang,Deadman, John Joseph,Xie, Xin,Ma, Dawei

, p. 5334 - 5336 (2010)

Modification of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists revealed that introducing a fluoro group at the 3-position of the 3-phenyl group to reduce metabolism did not adversely affect the high potency against HIV infection, and that replacing the piperidine ring with a tropane ring could deliver the most potent anti-HIV agents. Stereochemistry of the substituted tropane ring is essential for maintaining the potent anti-HIV activity because only exo-isomers displayed subnanomolar whole cell activity.

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