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CAS

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1369534-94-0

2-(4-bromophenoxy)-1,3-diacetoxypropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1369534-94-0 Structure

  • Basic information

    1. Product Name: 2-(4-bromophenoxy)-1,3-diacetoxypropane
    2. Synonyms: 2-(4-bromophenoxy)-1,3-diacetoxypropane
    3. CAS NO:1369534-94-0
    4. Molecular Formula:
    5. Molecular Weight: 331.163
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1369534-94-0.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: 2-(4-bromophenoxy)-1,3-diacetoxypropane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-bromophenoxy)-1,3-diacetoxypropane(1369534-94-0)
    11. EPA Substance Registry System: 2-(4-bromophenoxy)-1,3-diacetoxypropane(1369534-94-0)

  • 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: 1369534-94-0(Hazardous Substances Data)

1369534-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369534-94-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,5,3 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1369534-94:
(9*1)+(8*3)+(7*6)+(6*9)+(5*5)+(4*3)+(3*4)+(2*9)+(1*4)=200
200 % 10 = 0
So 1369534-94-0 is a valid CAS Registry Number.

1369534-94-0Relevant 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)

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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