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CAS

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81000-66-0

Boc-His(Dnp)-Pro-Lac-OBzl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81000-66-0 Structure

  • Basic information

    1. Product Name: Boc-His(Dnp)-Pro-Lac-OBzl
    2. Synonyms:
    3. CAS NO:81000-66-0
    4. Molecular Formula:
    5. Molecular Weight: 680.671
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81000-66-0.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: Boc-His(Dnp)-Pro-Lac-OBzl(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-His(Dnp)-Pro-Lac-OBzl(81000-66-0)
    11. EPA Substance Registry System: Boc-His(Dnp)-Pro-Lac-OBzl(81000-66-0)

  • 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: 81000-66-0(Hazardous Substances Data)

81000-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81000-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81000-66:
(7*8)+(6*1)+(5*0)+(4*0)+(3*0)+(2*6)+(1*6)=80
80 % 10 = 0
So 81000-66-0 is a valid CAS Registry Number.

81000-66-0Relevant articles and documents

Synthesis of Angiotensin II Antagonists with Variations in Position 5

Nyeki, Olga,Szalay, Katalin Sz.,Kisfaludy, Lajos,Karpati, Egon,Szporny, Laszlo,et al.

, p. 1719 - 1724 (2007/10/02)

Six angiotensin II antagonists containing cyclohexylglycine (Chg) or cyclopentylglycine (Cpg) in position 5 were synthesized by stepwise elongation in solution, using the pentafluorophenyl ester method.The influence of substitution on the inhibitory prope

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