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1173243-67-8

C32H35N3O8 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1173243-67-8 Structure

  • Basic information

    1. Product Name: C32H35N3O8
    2. Synonyms:
    3. CAS NO:1173243-67-8
    4. Molecular Formula:
    5. Molecular Weight: 589.645
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1173243-67-8.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: C32H35N3O8(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H35N3O8(1173243-67-8)
    11. EPA Substance Registry System: C32H35N3O8(1173243-67-8)

  • 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: 1173243-67-8(Hazardous Substances Data)

1173243-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173243-67-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,4 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1173243-67:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*4)+(3*3)+(2*6)+(1*7)=138
138 % 10 = 8
So 1173243-67-8 is a valid CAS Registry Number.

1173243-67-8Upstream product

1173243-67-8Downstream Products

1173243-67-8Relevant articles and documents

Total synthesis of the epimer at C-6′ of the miharamycin B framework

Marcelo, Filipa,Abou-Jneid, Robert,Sollogoub, Matthieu,Marrot, Jér?me,Rauter, Amélia P.,Blériot, Yves

, p. 1269 - 1272 (2009)

The total synthesis of the epimer at C-6′ of the core of the complex nucleoside antibiotic miharamycin B is reported. Optimization of the N-glycosylation key step involving the atypical 2-aminopurine nucleobase and a bicyclic glycosyl donor enabled to acc

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