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201139-12-0

C33H40ClN2O9P is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 201139-12-0 Structure

  • Basic information

    1. Product Name: C33H40ClN2O9P
    2. Synonyms: C33H40ClN2O9P
    3. CAS NO:201139-12-0
    4. Molecular Formula:
    5. Molecular Weight: 675.115
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201139-12-0.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: C33H40ClN2O9P(CAS DataBase Reference)
    10. NIST Chemistry Reference: C33H40ClN2O9P(201139-12-0)
    11. EPA Substance Registry System: C33H40ClN2O9P(201139-12-0)

  • 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: 201139-12-0(Hazardous Substances Data)

201139-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201139-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,1,3 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201139-12:
(8*2)+(7*0)+(6*1)+(5*1)+(4*3)+(3*9)+(2*1)+(1*2)=70
70 % 10 = 0
So 201139-12-0 is a valid CAS Registry Number.

201139-12-0Relevant articles and documents

'Armed-disarmed' glycosidation strategy based on glycosyl donors and acceptors carrying phosphoroamidate as a leaving group: A convergent synthesis of globotriaosylceramide

Hashimoto, Shun-Ichi,Sakamoto, Hiroki,Honda, Takeshi,Abe, Hiroshi,Nakamura, Sei-Ichi,Ikegami, Shiro

, p. 8969 - 8972 (2007/10/03)

A stereocontrolled synthesis of globotriaosylceramide with three different glycosidic linkages has been accomplished by linear and convergent routes exploiting 'armed-disarmed' glycosidation methodology based on glycosyl donors and acceptors carrying tetramethylphosphoroamidate as a leaving group. In particular, the convergent strategy featuring a coupling of a galactosyl(1→4)-galactosyl donor with a glucosylceramide derivative has proven to be extremely efficient.

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