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165065-03-2

7-deoxy-7-α-azido-paclitaxel is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 165065-03-2 Structure

  • Basic information

    1. Product Name: 7-deoxy-7-α-azido-paclitaxel
    2. Synonyms: 7-deoxy-7-α-azido-paclitaxel
    3. CAS NO:165065-03-2
    4. Molecular Formula:
    5. Molecular Weight: 878.933
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 165065-03-2.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: 7-deoxy-7-α-azido-paclitaxel(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-deoxy-7-α-azido-paclitaxel(165065-03-2)
    11. EPA Substance Registry System: 7-deoxy-7-α-azido-paclitaxel(165065-03-2)

  • 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: 165065-03-2(Hazardous Substances Data)

165065-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165065-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,0,6 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 165065-03:
(8*1)+(7*6)+(6*5)+(5*0)+(4*6)+(3*5)+(2*0)+(1*3)=122
122 % 10 = 2
So 165065-03-2 is a valid CAS Registry Number.

165065-03-2Downstream Products

165065-03-2Relevant articles and documents

Synthesis and Biological Evaluation of Paclitaxel Analogs Modified in Ring C

Liang, Xian,Kingston, David G. I.,Lin, Chii M.,Hamel, Ernest

, p. 2901 - 2904 (1995)

Both 7-deoxy-7α-azidopaclitaxel (6) and 7-deoxy-Δ6,7-paclitaxel (4) can be prepared from paclitaxel-7-O-triflate (2b).Oxidation of 7-deoxy-Δ6,7-paclitaxel with dioxirane yields the epoxide 7, while oxidation with osmium tetroxide yie

Synthesis and Molecular Modeling of Taxanes Modified at Ring C

Menichincheri, Maria,Botta, Maurizio,Ceccarelli, Walter,Ciomei, Marina,Corelli, Federico,et al.

, p. 534 - 556 (2007/10/03)

Some new paclitaxel analogs, modified at ring C, - namely the 7-α-mesylate, 7-deoxy-7-α-amino, 4-deacetoxy-4α-hydroxy-4β-hydroxymethyl-5α-acetoxy-Δ6,7-20-O-seco and 4-deacetoxy-4α-hydroxy-4β-hydroxymethyl-5α-acetoxy-6,7-epoxy-20-O-seco derivatives - are presented. The biological activity of 4-deacetoxy-4α-hydroxy-4β-hydroxymethyl-5α-acetoxy-Δ6,7-20-O-seco, 4-deacetoxy-4α-hydroxy-4β-hydroxymethyl-5α-acetoxy-6,7-epoxy-20-O-seco, 7-deoxy-7-α-azido, 7-deoxy-7-α-amino and 6,7-epoxy derivatives heve been evaluated. A molecular modeling study on some paclitaxel derivatives has been done in an attempt to rationalize the difference in biological activity.

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