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(R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 885022-10-6 Structure
  • Basic information

    1. Product Name: (R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester
    2. Synonyms: (R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester
    3. CAS NO:885022-10-6
    4. Molecular Formula:
    5. Molecular Weight: 397.471
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885022-10-6.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: (R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester(885022-10-6)
    11. EPA Substance Registry System: (R)-N-tert-butoxycarbonyl-4-benzoylphenylalaninol acetic acid ester(885022-10-6)
  • 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: 885022-10-6(Hazardous Substances Data)

885022-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885022-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,0,2 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 885022-10:
(8*8)+(7*8)+(6*5)+(5*0)+(4*2)+(3*2)+(2*1)+(1*0)=166
166 % 10 = 6
So 885022-10-6 is a valid CAS Registry Number.

885022-10-6Upstream product

885022-10-6Relevant articles and documents

Development of the first potential covalent inhibitors of anandamide cellular uptake

Moriello, Aniello Schiano,Balas, Laurence,Ligresti, Alessia,Cascio, Maria Grazia,Durand, Thierry,Morera, Enrico,Ortar, Giorgio,Di Marzo, Vincenzo

, p. 2320 - 2332 (2006)

On the basis of the chemical structures of two previously developed metabolically stable and relatively potent inhibitors of anandamide uptake, OMDM-1,2, two series of potential covalent inhibitors of anandamide cellular reuptake, which might be used for the molecular characterization of the protein(s) involved in the membrane transport of endocannabinoids, have been designed and synthesized. Most of the compounds inhibited uptake to a varied extent and in a generally enantio-sensitive manner when co-incubated with [ 14C]anandamide, but only three of them, the photoactivatable 1a (OMDM-37), 1b (OMDM-39), and 8 (Lo395), also produced a significant inhibition of uptake following the preincubation only of the cells, and this effect was significantly enhanced following UV exposure only in the case of 8. None of the new compounds inhibited [14C]anandamide hydrolysis with IC 50 50 μM, except for 1b.

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