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C42H59N5O9 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1219818-13-9 Structure
  • Basic information

    1. Product Name: C42H59N5O9
    2. Synonyms: C42H59N5O9
    3. CAS NO:1219818-13-9
    4. Molecular Formula:
    5. Molecular Weight: 777.959
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1219818-13-9.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: C42H59N5O9(CAS DataBase Reference)
    10. NIST Chemistry Reference: C42H59N5O9(1219818-13-9)
    11. EPA Substance Registry System: C42H59N5O9(1219818-13-9)
  • 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: 1219818-13-9(Hazardous Substances Data)

1219818-13-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219818-13-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,8,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1219818-13:
(9*1)+(8*2)+(7*1)+(6*9)+(5*8)+(4*1)+(3*8)+(2*1)+(1*3)=159
159 % 10 = 9
So 1219818-13-9 is a valid CAS Registry Number.

1219818-13-9Downstream Products

1219818-13-9Relevant articles and documents

OLIGOOXOPIPERAZINES AND METHODS OF MAKING AND USING THEM

-

, (2012/03/08)

The present invention relates to oligooxopiperazines and their use. Methods for preparing oligooxopiperazines are also disclosed.

Oligooxopiperazines as nonpeptidic α-helix mimetics

Tosovska, Petra,Arora, Paramjit S.

supporting information; experimental part, p. 1588 - 1591 (2010/06/16)

Chemical Reaction Repretatio A new class of nonpeptidic α-helix mlmetics derived from a-amino acids and featuring chlral backbones is described. NMR and circular dichroism spectroscopies, in combination with molecular modeling studies, provide compelling evidence that ollgooxopiperazlne dimers adopt stable conformations that reproduce the arrangement of i, i+4, and i+7 residues on an α-helix.

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