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112068-33-4

Butanoic acid, 3-(phenylmethoxy)-, ethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112068-33-4 Structure

  • Basic information

    1. Product Name: Butanoic acid, 3-(phenylmethoxy)-, ethyl ester, (S)-
    2. Synonyms:
    3. CAS NO:112068-33-4
    4. Molecular Formula: C13H18O3
    5. Molecular Weight: 222.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112068-33-4.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: Butanoic acid, 3-(phenylmethoxy)-, ethyl ester, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanoic acid, 3-(phenylmethoxy)-, ethyl ester, (S)-(112068-33-4)
    11. EPA Substance Registry System: Butanoic acid, 3-(phenylmethoxy)-, ethyl ester, (S)-(112068-33-4)

  • 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: 112068-33-4(Hazardous Substances Data)

112068-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112068-33-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,6 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112068-33:
(8*1)+(7*1)+(6*2)+(5*0)+(4*6)+(3*8)+(2*3)+(1*3)=84
84 % 10 = 4
So 112068-33-4 is a valid CAS Registry Number.

112068-33-4Relevant articles and documents

A Unified Synthetic Approach to Optically Pure Curvularin-Type Metabolites

Allu, Srinivasa Rao,Banne, Sreenivas,Jiang, Jia,Qi, Na,Guo, Jian,He, Yun

, p. 7227 - 7237 (2019)

A unified and concise approach to the synthesis of nine curvularin-type metabolites and two analogues has been developed with few steps and high yields. Among them, sumalactones A-D were synthesized for the first time. The key steps in this approach inclu

Enantioselective epoxidation of unfunctionalized simple olefins by non-racemic molybdenum(VI)(oxo-diperoxo) complexes

Schurig, V.,Hintzer, K.,Leyrer, U.,Mark, C.,Pitchen, P.,Kagan, H. B.

, p. 81 - 96 (2007/10/02)

Molybdenum(VI)(oxo-diperoxo) complexes bearing bidentate ligands with hydroxy and carbonyl functions show asymmetric induction in the stoichiometric epoxidation of simple prochiral olefins.The influence of the ligand and alkene structure on the enantiomeric excess of the oxiranes has been investigated.The addition of chiral diols to the molybdenum(VI)(oxo-diperoxo) reagents gives high enantiomeric excesses probably because of an efficient kinetic resolution of the oxiranes formed.

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