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CAS

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1285718-94-6

(2R,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1285718-94-6 Structure

  • Basic information

    1. Product Name: (2R,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one
    2. Synonyms: (2R,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one
    3. CAS NO:1285718-94-6
    4. Molecular Formula:
    5. Molecular Weight: 244.314
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1285718-94-6.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,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one(1285718-94-6)
    11. EPA Substance Registry System: (2R,3S)-2,3-epoxy-1-(2-thienyl)-3-(2-tolyl)-propan-1-one(1285718-94-6)

  • 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: 1285718-94-6(Hazardous Substances Data)

1285718-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1285718-94-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,5,7,1 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1285718-94:
(9*1)+(8*2)+(7*8)+(6*5)+(5*7)+(4*1)+(3*8)+(2*9)+(1*4)=196
196 % 10 = 6
So 1285718-94-6 is a valid CAS Registry Number.

1285718-94-6Downstream Products

1285718-94-6Relevant articles and documents

Enantioselective synthesis of heteroaromatic epoxyketones under phase-transfer catalysis using D-glucose- and D-mannose-based crown ethers

Rapi, Zsolt,Szabo, Tamas,Keglevich, Gyoergy,Szxoellosy, Aron,Drahos, Laszlo,Bako, Peter

, p. 1189 - 1196 (2011)

Heteroaromatic epoxyketones have been synthesized in an asymmetric Darzens condensation of 2-chloroacetylfuran or 2- and 3-chloroacetylthiophene with aromatic aldehydes and in the enantioselective epoxidation of α,β-enones with an N-methylpyrrole unit, in

Asymmetric C-C bond formation via Darzens condensation and Michael addition using monosaccharide-based chiral crown ethers

Bakó, Péter,Rapi, Zsolt,Keglevich, Gy?rgy,Szabó, Tamás,Sóti, Péter L.,Vígh, Tamás,Grn, Alajos,Holczbauer, Tamás

experimental part, p. 1473 - 1476 (2011/06/10)

Liquid-liquid phase asymmetric Darzens condensations were promoted by d-glucose- and d-mannose-based crown ethers. The corresponding aromatic and heteroaromatic α,β-epoxyketones were obtained with moderate to high enantioselectivities (up to 96%) as well

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