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1608495-58-4

C57H69N3O6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1608495-58-4 Structure

  • Basic information

    1. Product Name: C57H69N3O6
    2. Synonyms: C57H69N3O6
    3. CAS NO:1608495-58-4
    4. Molecular Formula:
    5. Molecular Weight: 892.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608495-58-4.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: C57H69N3O6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C57H69N3O6(1608495-58-4)
    11. EPA Substance Registry System: C57H69N3O6(1608495-58-4)

  • 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: 1608495-58-4(Hazardous Substances Data)

1608495-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608495-58-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,4,9 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1608495-58:
(9*1)+(8*6)+(7*0)+(6*8)+(5*4)+(4*9)+(3*5)+(2*5)+(1*8)=194
194 % 10 = 4
So 1608495-58-4 is a valid CAS Registry Number.

1608495-58-4Upstream product

1608495-58-4Downstream Products

1608495-58-4Relevant articles and documents

Complexation-induced inversion of helicity by an organic guest in a dynamic molecular propeller based on a tristerephthalamide host with a two-layer structure

Katoono, Ryo,Fujiwara, Kenshu,Suzuki, Takanori

, p. 5438 - 5440 (2014)

A tristerephthalamide host exhibited two helical geometries with (M)- and (P)-helicity, respectively, in terms of the twisting direction of a two-layer structure, and the helical preference switched upon complexation with a ditopic guest. In both uncomplexed and complexed states, the intramolecular transmission of chirality was responsible for the control of helicity. This journal is the Partner Organisations 2014.

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