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130306-76-2

PhTX-343-L-lysine amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130306-76-2 Structure

  • Basic information

    1. Product Name: PhTX-343-L-lysine amide
    2. Synonyms: PhTX-343-L-lysine amide
    3. CAS NO:130306-76-2
    4. Molecular Formula:
    5. Molecular Weight: 563.784
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130306-76-2.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: PhTX-343-L-lysine amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: PhTX-343-L-lysine amide(130306-76-2)
    11. EPA Substance Registry System: PhTX-343-L-lysine amide(130306-76-2)

  • 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: 130306-76-2(Hazardous Substances Data)

130306-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130306-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,0 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130306-76:
(8*1)+(7*3)+(6*0)+(5*3)+(4*0)+(3*6)+(2*7)+(1*6)=82
82 % 10 = 2
So 130306-76-2 is a valid CAS Registry Number.

130306-76-2Downstream Products

130306-76-2Relevant articles and documents

Side-chain-anchored Nα-Fmoc-Tyr-OPfp for bidirectional solid-phase synthesis

Olsen, Christian A.,Jorgensen, Malene R.,Hansen, Steen H.,Witt, Matthias,Jaroszewski, Jerzy W.,Franzyk, Henrik

, p. 1703 - 1706 (2007/10/03)

(Chemical Equation Presented) A mild resin-immobilization strategy employing a readily prepared trityl bromide resin for anchoring building blocks via a phenol group has been developed. With Nα-Fmoc-Tyr-OPfp as a starter building block, it was possible to prepare asymmetrically substituted hybrids of spider-and wasp-type polyamine toxins using solid-phase peptide synthesis conditions.

Synthesis and binding of [125I2]philanthotoxin-343, [125I2]philanthotoxin-343-lysine, and [125I2]philanthotoxin-343-arginine to rat brain membranes

Goodnow Jr.,Bukownik,Nakanishi,Usherwood,Eldefrawi,Anis,Eldefrawi

, p. 2389 - 2394 (2007/10/02)

125I2-iodinated philanthotoxin-343 (PhTX-343) (10), [125I2]PhTX-343-arginine (11), and [125I2]PhTX-343-lysine (12) were synthesized and evaluated as probes for glutamate receptors in rat br

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