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1194396-99-0

C32H50N6O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1194396-99-0 Structure

  • Basic information

    1. Product Name: C32H50N6O
    2. Synonyms:
    3. CAS NO:1194396-99-0
    4. Molecular Formula:
    5. Molecular Weight: 534.789
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1194396-99-0.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: C32H50N6O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H50N6O(1194396-99-0)
    11. EPA Substance Registry System: C32H50N6O(1194396-99-0)

  • 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: 1194396-99-0(Hazardous Substances Data)

1194396-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194396-99-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,3,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1194396-99:
(9*1)+(8*1)+(7*9)+(6*4)+(5*3)+(4*9)+(3*6)+(2*9)+(1*9)=200
200 % 10 = 0
So 1194396-99-0 is a valid CAS Registry Number.

1194396-99-0Downstream Products

1194396-99-0Relevant articles and documents

Enlarged analogues of uniconazole, new azole containing inhibitors of ABA 8′-hydroxylase CYP707A

Todoroki, Yasushi,Aoyama, Hikaru,Hiramatsu, Saori,Shirakura, Minaho,Nimitkeatkai, Hataitip,Kondo, Satoru,Ueno, Kotomi,Mizutani, Masaharu,Hirai, Nobuhiro

experimental part, p. 5782 - 5786 (2010/04/25)

We enlarged the uniconazole (UNI) molecule to find a specific inhibitor of abscisic acid (ABA) 8′-hydroxylase, and synthesized various UNI derivatives that were substituted with hydrophilic and hydrophobic groups at the 4-chlorine of the phenyl group of U

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