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207680-02-2

10-isobutyloyl 10-deacetylbaccatin III is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 207680-02-2 Structure

  • Basic information

    1. Product Name: 10-isobutyloyl 10-deacetylbaccatin III
    2. Synonyms: 10-isobutyloyl 10-deacetylbaccatin III
    3. CAS NO:207680-02-2
    4. Molecular Formula:
    5. Molecular Weight: 614.69
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207680-02-2.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: 10-isobutyloyl 10-deacetylbaccatin III(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-isobutyloyl 10-deacetylbaccatin III(207680-02-2)
    11. EPA Substance Registry System: 10-isobutyloyl 10-deacetylbaccatin III(207680-02-2)

  • 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: 207680-02-2(Hazardous Substances Data)

207680-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207680-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,6,8 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 207680-02:
(8*2)+(7*0)+(6*7)+(5*6)+(4*8)+(3*0)+(2*0)+(1*2)=122
122 % 10 = 2
So 207680-02-2 is a valid CAS Registry Number.

207680-02-2Relevant articles and documents

Lanthanide trifluoromethanesulfonate catalysed selective acylation of 10-deacetylbaccatin III

Damen, Eric W. P.,Braamer, Lesly,Scheeren, Hans W.

, p. 6081 - 6082 (1998)

The selective C-10 acylation of 10-deacetylbaccatin III to baccatin III and derivatives is very efficiently catalysed by lanthanide trifluoromethanesulfonates. Baccatin III, now readily available through this procedure, is an important precursor for an economically viable semisynthesis of paclitaxel and its derivatives.

Organocatalytic site-selective acylation of 10-deacetylbaccatin III

Yanagi, Masanori,Ninomiya, Ryo,Ueda, Yoshihiro,Furuta, Takumi,Yamada, Takeshi,Sunazuka, Toshiaki,Kawabata, Takeo

, p. 907 - 912 (2016/07/14)

Organocatalytic site-selective diversification of 10-deacetylbaccatin III, a key natural product for the semisynthesis of taxol, has been achieved. Various acyl groups were selectively introduced into the C(10)-OH of 10-deacetylbaccatin III. The C(10)-OH selective acylation was also applied to acylative site-selective dimerization of 10-deacetylbaccatin III to provide the structurally defined dimer.

Synthesis and biological evaluation of C-3′NH/C-10 and C-2/C-10 modified paclitaxel analogues

Baloglu, Erkan,Hoch, Jeannine M.,Chatterjee, Sabarni K.,Ravindra, Rudravajhala,Bane, Susan,Kingston, David G. I.

, p. 1557 - 1568 (2007/10/03)

Concurrent modifications on the C-3′NH/C-10, and C-2/C-10 positions on paclitaxel were carried out as a way of investigating possible synergistic effects. The biological activities of these analogues were evaluated in both a microtubule assembly assay and

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