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790664-66-3

3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 790664-66-3 Structure

  • Basic information

    1. Product Name: 3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol
    2. Synonyms: 3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol
    3. CAS NO:790664-66-3
    4. Molecular Formula:
    5. Molecular Weight: 208.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 790664-66-3.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: 3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol(790664-66-3)
    11. EPA Substance Registry System: 3-[1-benzyloxy-(1S)-ethyl]-(2R,3S)-oxiran-2-yl methanol(790664-66-3)

  • 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: 790664-66-3(Hazardous Substances Data)

790664-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 790664-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,6,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 790664-66:
(8*7)+(7*9)+(6*0)+(5*6)+(4*6)+(3*4)+(2*6)+(1*6)=203
203 % 10 = 3
So 790664-66-3 is a valid CAS Registry Number.

790664-66-3Relevant articles and documents

Flexible and simple route for the stereoselective synthesis of trisubstituted γ-butyrolactones: Total synthesis of (+)-blastomycinone and its analogs

Krishna, Palakodety Radha,Reddy, V. V. Ramana,Sharma

, p. 2107 - 2114 (2004)

A flexible route for the stereoselective synthesis of trisubstituted γ-butyrolactones, namely (+)-blastomycinone and its analogs, is devised by the Sharpless asymmetric epoxidation and the regioselective ring opening reaction with dibutylcopper lithium as

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