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t-Bumeoc-L-Phe-D-Leu-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85313-56-0 Structure
  • Basic information

    1. Product Name: t-Bumeoc-L-Phe-D-Leu-OH
    2. Synonyms:
    3. CAS NO:85313-56-0
    4. Molecular Formula:
    5. Molecular Weight: 552.755
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85313-56-0.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: t-Bumeoc-L-Phe-D-Leu-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: t-Bumeoc-L-Phe-D-Leu-OH(85313-56-0)
    11. EPA Substance Registry System: t-Bumeoc-L-Phe-D-Leu-OH(85313-56-0)
  • 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: 85313-56-0(Hazardous Substances Data)

85313-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85313-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,1 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85313-56:
(7*8)+(6*5)+(5*3)+(4*1)+(3*3)+(2*5)+(1*6)=130
130 % 10 = 0
So 85313-56-0 is a valid CAS Registry Number.

85313-56-0Relevant articles and documents

The 1-(3,5-Di-tert-butylphenyl)-1-methylethoxycarbonyl (t-Bumeoc) Residue, a Protecting Group Cleavable under Extremely Mild Acidic Conditions

Voelter, Wolfgang,Mueller, Juergen

, p. 248 - 260 (2007/10/02)

The synthesis of 1-(3,5-di-tert-butylphenyl)-1-methylethoxycarbonyl fluoride (8) and its reaction with selected amino acids as well as the 13C NMR spectroscopic characterization of t-Bumeoc derivatives are described.The new protecting group is cleavable under very mild acidic conditions.The kinetics of the cleavage is studied by high-performance liquid chromatography (HPLC).The utility of the t-Bumeoc compared to the Adpoc protecting group is demonstrated taking a derivative of the molluscan neuropeptide as an example.

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