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24,33-Bis-(t.butyl-dimethylsilyl)-Δ10-FK 506 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144895-55-6 Structure
  • Basic information

    1. Product Name: 24,33-Bis-(t.butyl-dimethylsilyl)-Δ10-FK 506
    2. Synonyms:
    3. CAS NO:144895-55-6
    4. Molecular Formula:
    5. Molecular Weight: 1000.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144895-55-6.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: 24,33-Bis-(t.butyl-dimethylsilyl)-Δ10-FK 506(CAS DataBase Reference)
    10. NIST Chemistry Reference: 24,33-Bis-(t.butyl-dimethylsilyl)-Δ10-FK 506(144895-55-6)
    11. EPA Substance Registry System: 24,33-Bis-(t.butyl-dimethylsilyl)-Δ10-FK 506(144895-55-6)
  • 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: 144895-55-6(Hazardous Substances Data)

144895-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144895-55-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,9 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144895-55:
(8*1)+(7*4)+(6*4)+(5*8)+(4*9)+(3*5)+(2*5)+(1*5)=166
166 % 10 = 6
So 144895-55-6 is a valid CAS Registry Number.

144895-55-6Downstream Products

144895-55-6Relevant articles and documents

Synthesis of Derivatives of FK 506 and FR 900520: Modifications at the Binding Domain

Emmer, Gerhard,Weber-Roth, Sabine

, p. 5861 - 5874 (1992)

The synthesis of 9-deoxo-FK 506 (13a), 9-deoxo-FR 900520 (13b), 9-deoxo-10(R)-deoxy-FR900520 (14) and its 10(S) isomer 15 is described.Radical deoxygenation/elimination of the 9-dihydro-9,10-thiocarbonates 5a,5b,6a and 6b gave the 9,10 unsaturated compoun

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