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83824-97-9

N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83824-97-9 Structure

  • Basic information

    1. Product Name: N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide
    2. Synonyms: N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide
    3. CAS NO:83824-97-9
    4. Molecular Formula:
    5. Molecular Weight: 801.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83824-97-9.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: N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide(83824-97-9)
    11. EPA Substance Registry System: N,N-ditetradecyl-Nα-t-butoxycarbonyl-Nim-tosyl-L-histidinamide(83824-97-9)

  • 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: 83824-97-9(Hazardous Substances Data)

83824-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83824-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,2 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83824-97:
(7*8)+(6*3)+(5*8)+(4*2)+(3*4)+(2*9)+(1*7)=159
159 % 10 = 9
So 83824-97-9 is a valid CAS Registry Number.

83824-97-9Relevant articles and documents

Catalytic Efficiency of Functionalized Vesicles in the Transamination of Pyridoxal-5'-phosphate with a Hydrophobic Amino Acid

Murakami, Yukito,Nakano, Akio,Akiyoshi, Kazunari

, p. 3004 - 3012 (1982)

The transamination reaction of pyridoxal-5'-phosphate (PLP) with N-dodecyl-L-alaninamide (AlaC12) was investigated in an aqueous phosphate-borate buffer at pH 7.0, μ 0.10 (KCl), and 30.0+/-0.1 deg C in the presence of single-walled vesicles of N,N-ditetradecyl-Nα-(6-trimethylammoniohexanoyl)-L-histidinamide bromide (N+C5His2C14).The electrostatic and hydrophobic interactions between the vesicles and the reactants resulted in incorporation of PLP and AlaC12 into polar and hydrophobic domains of the vesicles, respectively, in the Schiff-base formation process.The isomerization of the aldimine Schiff-base to the correspeonding ketimine Schiff-base was confirmed to be the rate-determining step in the transamination process.The reaction site in the vesicular system was found to be equivalent in polarity to dioxane-water (7:3 v/v).However, the overall reaction rate in the vesicles was enhanced 230-fold relative to that in dioxane-water (7:3 v/v).A hydrophobic and suitably polar microenvironment constructed at the reaction site is responsible for such a marked rate-enhancement.In addition, each vesicle of N+C5His2C14 provided functional (imidazolyl) groups in its hydrogen-belt domain to catalyze the intramolecular prototropic shift to yield the ketimine Schiff-base.The microenvironmental effects of molecular assemblies of N,N-ditetradecyl-Nα-(6-trimethylammoniohexanoyl)-L-alaninamide bromide and CTAB on the overall transamination were also discussed.

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