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1341219-73-5

C66H82N6O11Si2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1341219-73-5 Structure

  • Basic information

    1. Product Name: C66H82N6O11Si2
    2. Synonyms: C66H82N6O11Si2
    3. CAS NO:1341219-73-5
    4. Molecular Formula:
    5. Molecular Weight: 1191.58
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1341219-73-5.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: C66H82N6O11Si2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C66H82N6O11Si2(1341219-73-5)
    11. EPA Substance Registry System: C66H82N6O11Si2(1341219-73-5)

  • 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: 1341219-73-5(Hazardous Substances Data)

1341219-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1341219-73-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,1,2,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1341219-73:
(9*1)+(8*3)+(7*4)+(6*1)+(5*2)+(4*1)+(3*9)+(2*7)+(1*3)=125
125 % 10 = 5
So 1341219-73-5 is a valid CAS Registry Number.

1341219-73-5Relevant articles and documents

Development of the carboxamide protecting group, 4-(tert -butyldimethylsiloxy)-2-methoxybenzyl

Muranaka, Kazuhiro,Ichikawa, Satoshi,Matsuda, Akira

experimental part, p. 9278 - 9293 (2012/01/04)

The new carboxamide protecting group, 4-(tert-butyldimethylsiloxy)-2- methoxybenzyl (SiMB), has been developed. While this SiMB group can be removed using mild basic desilylation methods, it can also be deprotected under strongly acidic or oxidative conditions. An application of this group to simple carboxamide groups, as well as to more complex and acid-sensitive adenosine derivatives containing a cyclophane scaffold, was also demonstrated.

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