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Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130973-44-3 Structure
  • Basic information

    1. Product Name: Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI)
    2. Synonyms: Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI)
    3. CAS NO:130973-44-3
    4. Molecular Formula: C7H12O3
    5. Molecular Weight: 144.16838
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 130973-44-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI)(130973-44-3)
    11. EPA Substance Registry System: Ethanone, 1-[2-(1-hydroxypropyl)oxiranyl]-, (R*,S*)- (9CI)(130973-44-3)
  • 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: 130973-44-3(Hazardous Substances Data)

130973-44-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130973-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,7 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 130973-44:
(8*1)+(7*3)+(6*0)+(5*9)+(4*7)+(3*3)+(2*4)+(1*4)=123
123 % 10 = 3
So 130973-44-3 is a valid CAS Registry Number.

130973-44-3Downstream Products

130973-44-3Relevant articles and documents

Asymmetric metal-catalysed epoxidation of electron-deficient olefins

Bailey,Staton,Ashton,Marko,Ollis

, p. 495 - 509 (2007/10/02)

The SYN diastereospecific epoxidation of acyclic β-hydroxyketones (β-hydroxyacrylates) and cyclic β-hydroxyketones using titanium and vanadium catalysts is reported. Some initial results on the asymmetric epoxidation of these systems using the Sharpless t

Stereoselective epoxidation of hydroxyenones. The synthesis of the sidechain of clerocidin

Bailey,Marko,Ollis,Rasmussen

, p. 4509 - 4512 (2007/10/02)

The sidechains of clerocidin 1 and terpentecin 2 contain a unique chiral assembly [C5H5O4]. Models for the stereospecific synthesis of this structural feature are reported.

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