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(-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 881915-50-0 Structure
  • Basic information

    1. Product Name: (-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol
    2. Synonyms: (-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol
    3. CAS NO:881915-50-0
    4. Molecular Formula:
    5. Molecular Weight: 358.577
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 881915-50-0.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: (-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol(881915-50-0)
    11. EPA Substance Registry System: (-)-(2S,3S)-2-(tert-butyldiphenylsilanyloxymethyl)thietan-3-ol(881915-50-0)
  • 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: 881915-50-0(Hazardous Substances Data)

881915-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 881915-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,9,1 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 881915-50:
(8*8)+(7*8)+(6*1)+(5*9)+(4*1)+(3*5)+(2*5)+(1*0)=200
200 % 10 = 0
So 881915-50-0 is a valid CAS Registry Number.

881915-50-0Relevant articles and documents

Synthesis and anti-HIV activity of D- and L-thietanose nucleosides

Choo, Hyunah,Chen, Xin,Yadav, Vikas,Wang, Jianing,Schinazi, Raymond F.,Chu, Chung K.

, p. 1635 - 1647 (2006)

Various D- and L-thietanose nucleosides were synthesized from D- and L-xylose. The four-membered thietane ring was efficiently synthesized by the cyclization of 1-thioacetyl-3-mesylate (4/38) under basic conditions. Condensation with various heterocyclic

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