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1422163-40-3

C21(13)CH35NO3S2Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1422163-40-3 Structure

  • Basic information

    1. Product Name: C21(13)CH35NO3S2Si
    2. Synonyms:
    3. CAS NO:1422163-40-3
    4. Molecular Formula:
    5. Molecular Weight: 454.731
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1422163-40-3.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: C21(13)CH35NO3S2Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21(13)CH35NO3S2Si(1422163-40-3)
    11. EPA Substance Registry System: C21(13)CH35NO3S2Si(1422163-40-3)

  • 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: 1422163-40-3(Hazardous Substances Data)

1422163-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1422163-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,1,6 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1422163-40:
(9*1)+(8*4)+(7*2)+(6*2)+(5*1)+(4*6)+(3*3)+(2*4)+(1*0)=113
113 % 10 = 3
So 1422163-40-3 is a valid CAS Registry Number.

1422163-40-3Downstream Products

1422163-40-3Relevant articles and documents

Investigation of fungal iterative polyketide synthase functions using partially assembled intermediates

Gao, Zhizeng,Wang, Jingjing,Norquay, Amy K.,Qiao, Kangjian,Tang, Yi,Vederas, John C.

supporting information, p. 1735 - 1738 (2013/04/10)

Iterative polyketide synthases (PKSs) are large, multifunctional enzymes that resemble eukaryotic fatty acid synthases but can make highly functionalized secondary metabolites using complex and unresolved programming rules. During biosynthesis of the kinase inhibitor hypothemycin by Hypomyces subiculosus, a highly reducing iterative PKS, Hpm8, cooperates with a nonreducing iterative PKS, Hpm3, to construct the advanced intermediate dehydrozearalenol (DHZ). The identity of putative intermediates in the formation of the highly reduced hexaketide portion of DHZ were confirmed by incorporation of 13C-labeled N-acetylcysteamine (SNAC) thioesters using the purified enzymes. The results show that Hpm8 can accept SNAC thioesters of intermediates that are ready for transfer from its acyl carrier protein domain to its ketosynthase domain and assemble them into DHZ in cooperation with Hpm3. Addition of certain structurally modified analogues of intermediates to Hpm8 and Hpm3 can produce DHZ derivatives.

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