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  • 1002129-40-9 Structure
  • Basic information

    1. Product Name: C21H17F3O4
    2. Synonyms:
    3. CAS NO:1002129-40-9
    4. Molecular Formula:
    5. Molecular Weight: 390.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1002129-40-9.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: C21H17F3O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H17F3O4(1002129-40-9)
    11. EPA Substance Registry System: C21H17F3O4(1002129-40-9)
  • 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: 1002129-40-9(Hazardous Substances Data)

1002129-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1002129-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,1,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1002129-40:
(9*1)+(8*0)+(7*0)+(6*2)+(5*1)+(4*2)+(3*9)+(2*4)+(1*0)=69
69 % 10 = 9
So 1002129-40-9 is a valid CAS Registry Number.

1002129-40-9Relevant articles and documents

Discovery of novel 5,5-diarylpentadienamides as orally available transient receptor potential vanilloid 1 (TRPV1) antagonists

Saku, Osamu,Ishida, Hiroshi,Atsumi, Eri,Sugimoto, Yoshiyuki,Kodaira, Hiroshi,Kato, Yoshimitsu,Shirakura, Shiro,Nakasato, Yoshisuke

, p. 3436 - 3451 (2012/06/04)

We have developed a novel and potent chemical series of 5,5-diphenylpentadienamides for targeting TRPV1 in vitro and in vivo. In this investigation, we examined a variety of replacements for the 5-position of dienamides with the goal of addressing issues related to pharmacokinetics. Our data suggest that substitution with alkoxy groups on the phenyl ring at the 5-position increases their ability to penetrate the blood-brain barrier. This investigation culminated in the discovery of compound (R)-36b, which showed a good pharmacokinetic profile. In vivo, compound (R)-36b was found to be effective at reversing mechanical allodynia in rats in a dose-dependent manner, and it reversed thermal hyperalgesia in a model of neuropathic pain induced by sciatic nerve injury.

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