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CAS

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688010-04-0

C56H99NO13Si2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 688010-04-0 Structure

  • Basic information

    1. Product Name: C56H99NO13Si2
    2. Synonyms: C56H99NO13Si2
    3. CAS NO:688010-04-0
    4. Molecular Formula:
    5. Molecular Weight: 1050.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 688010-04-0.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: C56H99NO13Si2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C56H99NO13Si2(688010-04-0)
    11. EPA Substance Registry System: C56H99NO13Si2(688010-04-0)

  • 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: 688010-04-0(Hazardous Substances Data)

688010-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 688010-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,8,0,1 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 688010-04:
(8*6)+(7*8)+(6*8)+(5*0)+(4*1)+(3*0)+(2*0)+(1*4)=160
160 % 10 = 0
So 688010-04-0 is a valid CAS Registry Number.

688010-04-0Downstream Products

688010-04-0Relevant articles and documents

Selective photochemical cleavage of an α-ketoamide in a highly functionalised macrolide ascomycin

Bulusu, Murty A.R.C.,Waldst?tten, Peter,Tricotett, Thomas,Schulz, Gerhard

, p. 2527 - 2530 (2004)

A novel photochemical amide cleavage reaction of (6S)-methoxyascomycin opening a pathway for the selective cleavage of the pipecolic acid, is described. The scope of this reaction with several analogues carrying suitable protecting groups is examined.

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