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CAS

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744198-92-3

(2R)-3-(phenylseleno)propane-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 744198-92-3 Structure

  • Basic information

    1. Product Name: (2R)-3-(phenylseleno)propane-1,2-diol
    2. Synonyms: (2R)-3-(phenylseleno)propane-1,2-diol
    3. CAS NO:744198-92-3
    4. Molecular Formula:
    5. Molecular Weight: 231.153
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 744198-92-3.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: (2R)-3-(phenylseleno)propane-1,2-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R)-3-(phenylseleno)propane-1,2-diol(744198-92-3)
    11. EPA Substance Registry System: (2R)-3-(phenylseleno)propane-1,2-diol(744198-92-3)

  • 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: 744198-92-3(Hazardous Substances Data)

744198-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744198-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,1,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 744198-92:
(8*7)+(7*4)+(6*4)+(5*1)+(4*9)+(3*8)+(2*9)+(1*2)=193
193 % 10 = 3
So 744198-92-3 is a valid CAS Registry Number.

744198-92-3Relevant articles and documents

Intramolecular addition of carbon radicals to aldehydes: synthesis of enantiopure tetrahydrofuran-3-ols

Tiecco, Marcello,Testaferri, Lorenzo,Marini, Francesca,Sternativo, Silvia,Santi, Claudio,Bagnoli, Luana,Temperini, Andrea

, p. 5482 - 5489 (2008/01/07)

A simple and efficient substrate-controlled asymmetric synthesis of enantiopure tetrahydrofuran-3-ols by a 5-exo-trig radical cyclization is described. This cyclization occurs when a δ-carbon radical adds intramolecularly to the carbonyl group of an aldeh

Ring-Closure Reactions through Intramolecular Displacement of the Phenylselenonyl Group by Nitrogen Nucleophiles: A New Stereospecific Synthesis of N-Tosyl and N-Benzoyl-1,3-oxazolidin-2-ones from β-Hydroxyalkyl Phenyl Selenides

Tiecco, Marcello,Testaferri, Lorenzo,Temperini, Andrea,Bagnoli, Luana,Marini, Francesca,Santi, Claudio

, p. 1752 - 1764 (2007/10/03)

A new and convenient method for the stereospecific synthesis of variously substituted 1,3-oxazolidin-2-ones from the easily available β-hydroxyalkyl phenyl selenides is presented. After transformation into the N-tosyl or N-benzoyl carbamates, the selenide

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