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(1S)-9,11,25,26-tetrahydro-1-hydroxyvitamin D3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122172-43-4 Structure
  • Basic information

    1. Product Name: (1S)-9,11,25,26-tetrahydro-1-hydroxyvitamin D3
    2. Synonyms:
    3. CAS NO:122172-43-4
    4. Molecular Formula:
    5. Molecular Weight: 396.613
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122172-43-4.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: (1S)-9,11,25,26-tetrahydro-1-hydroxyvitamin D3(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S)-9,11,25,26-tetrahydro-1-hydroxyvitamin D3(122172-43-4)
    11. EPA Substance Registry System: (1S)-9,11,25,26-tetrahydro-1-hydroxyvitamin D3(122172-43-4)
  • 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: 122172-43-4(Hazardous Substances Data)

122172-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122172-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,1,7 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122172-43:
(8*1)+(7*2)+(6*2)+(5*1)+(4*7)+(3*2)+(2*4)+(1*3)=84
84 % 10 = 4
So 122172-43-4 is a valid CAS Registry Number.

122172-43-4Relevant articles and documents

Synthesis and Biological Activity of 9,11-Dehydrovitamin D3 analogues: Stereoselctive Preparation of 6β-Vitamin D Vinylallenes and a Concise Enynol Synthesis for Preparing the A-Ring

Okamura, William H.,Aurrecoechea, J. Miguel,Gibbs, Richard A.,Norman, Anthony W.

, p. 4072 - 4083 (2007/10/02)

The Δ9(11)-unsaturated vitamin D analogues 5a and 5b are of biochemical interest because they are incapable of tautomerizing via a sigmatropic hydrogen shift to a previtamin structure related to 3 and also becouse they possess a perturbed

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