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1221572-07-1

C41H46F17N3O10S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1221572-07-1 Structure

  • Basic information

    1. Product Name: C41H46F17N3O10S
    2. Synonyms:
    3. CAS NO:1221572-07-1
    4. Molecular Formula:
    5. Molecular Weight: 1095.87
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1221572-07-1.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: C41H46F17N3O10S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C41H46F17N3O10S(1221572-07-1)
    11. EPA Substance Registry System: C41H46F17N3O10S(1221572-07-1)

  • 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: 1221572-07-1(Hazardous Substances Data)

1221572-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1221572-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,5,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1221572-07:
(9*1)+(8*2)+(7*2)+(6*1)+(5*5)+(4*7)+(3*2)+(2*0)+(1*7)=111
111 % 10 = 1
So 1221572-07-1 is a valid CAS Registry Number.

1221572-07-1Relevant articles and documents

Use of cyclohexylisocyanide and methyl 2-isocyanoacetate as convertible isocyanides for microwave-assisted fluorous synthesis of 1,4-benzodiazepine-2,5- dione library

Zhou, Hongyu,Zhang, Wei,Yan, Bing

, p. 206 - 214 (2010)

A new protocol in which cyclohexylisocyanide and methyl 2-isocyanoacetate are used as convertible isocyanides for Ugi/de-Boc/cyclization/Suzuki synthesis of biaryl-substituted 1,4-benzodiazepine-2,5-diones has been developed. Ugi reactions of Boc-protecte

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