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83160-08-1

Nα-Tos-D-Orn-Gly-Phe-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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  • 83160-08-1 Structure

  • Basic information

    1. Product Name: Nα-Tos-D-Orn-Gly-Phe-Leu-OH
    2. Synonyms: Nα-Tos-D-Orn-Gly-Phe-Leu-OH
    3. CAS NO:83160-08-1
    4. Molecular Formula:
    5. Molecular Weight: 603.74
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83160-08-1.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: Nα-Tos-D-Orn-Gly-Phe-Leu-OH(CAS DataBase Reference)
    10. NIST Chemistry Reference: Nα-Tos-D-Orn-Gly-Phe-Leu-OH(83160-08-1)
    11. EPA Substance Registry System: Nα-Tos-D-Orn-Gly-Phe-Leu-OH(83160-08-1)

  • 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: 83160-08-1(Hazardous Substances Data)

83160-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83160-08-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,6 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83160-08:
(7*8)+(6*3)+(5*1)+(4*6)+(3*0)+(2*0)+(1*8)=111
111 % 10 = 1
So 83160-08-1 is a valid CAS Registry Number.

83160-08-1Relevant articles and documents

Synthesis and Pharmacological Characterization in Vitro of Cyclic Enkephalin Analogues: Effect of Conformational Constraints on Opiate Receptor Selectivity

DiMaio, John,Nguyen, Thi M.-D.,Lemieux, Carole,Schiller, Peter W.

, p. 1432 - 1438 (2007/10/02)

Using a combination of solid-phase and solution methods, we synthesized a series of cyclic 5> enkephalin analogues by substitution of D-α,ω-diamino acids in position 2 of the enkephalin sequence and cyclization of the ω-amino group to the C

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