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152769-09-0

Boc-(R)-Amhn-Lys(Z)-Gly-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 152769-09-0 Structure

  • Basic information

    1. Product Name: Boc-(R)-Amhn-Lys(Z)-Gly-OMe
    2. Synonyms: Boc-(R)-Amhn-Lys(Z)-Gly-OMe
    3. CAS NO:152769-09-0
    4. Molecular Formula:
    5. Molecular Weight: 638.761
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152769-09-0.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-(R)-Amhn-Lys(Z)-Gly-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: Boc-(R)-Amhn-Lys(Z)-Gly-OMe(152769-09-0)
    11. EPA Substance Registry System: Boc-(R)-Amhn-Lys(Z)-Gly-OMe(152769-09-0)

  • 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: 152769-09-0(Hazardous Substances Data)

152769-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152769-09-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,7,6 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 152769-09:
(8*1)+(7*5)+(6*2)+(5*7)+(4*6)+(3*9)+(2*0)+(1*9)=150
150 % 10 = 0
So 152769-09-0 is a valid CAS Registry Number.

152769-09-0Downstream Products

152769-09-0Relevant articles and documents

Template-Assembled Synthetic Proteins (TASP). Cyclic Templates with Incorporated Turn-Inducing Mimics

Ernest, Ivan,Kalvoda, Jaroslav,Sigel, Christoph,Rihs, Grety,Fritz, Hans,et al.

, p. 1539 - 1563 (2007/10/02)

The 8-amino-5,6,7,8-tetrahydronaphth-2-oic acid (1), 8-(aminomethyl)-5,6,7,8-tetrahydronaphth-2-oic acid (2), and 8-(aminomethyl)naphth-2-oic acid (3) were synthesized in their protected forms as turn-inducing dipeptide mimics.Two of them (2 and 3) were i

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