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118535-73-2

2-oxo-1,3-diphenylpropyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118535-73-2 Structure

  • Basic information

    1. Product Name: 2-oxo-1,3-diphenylpropyl acetate
    2. Synonyms: 2-oxo-1,3-diphenylpropyl acetate
    3. CAS NO:118535-73-2
    4. Molecular Formula:
    5. Molecular Weight: 268.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118535-73-2.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: 2-oxo-1,3-diphenylpropyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-oxo-1,3-diphenylpropyl acetate(118535-73-2)
    11. EPA Substance Registry System: 2-oxo-1,3-diphenylpropyl acetate(118535-73-2)

  • 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: 118535-73-2(Hazardous Substances Data)

118535-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118535-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,3 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118535-73:
(8*1)+(7*1)+(6*8)+(5*5)+(4*3)+(3*5)+(2*7)+(1*3)=132
132 % 10 = 2
So 118535-73-2 is a valid CAS Registry Number.

118535-73-2Downstream Products

118535-73-2Relevant articles and documents

Al Lewis acid-catalyzed regiodivergent 1,2-rearrangement of α-siloxy aldehydes: scope and mechanism

Ohmatsu, Kohsuke,Tanaka, Takayuki,Ooi, Takashi,Maruoka, Keiji

experimental part, p. 7516 - 7522 (2009/12/04)

Regiodivergent 1,2-rearrangement of α-siloxy aldehydes bearing α-aryl and α-alkyl substituents into α-siloxy ketones has been realized by using different Al Lewis acid catalyst/solvent systems. The scope of this unprecedented protocol has been investigate

Complete switch of migratory aptitude in aluminum-catalyzed 1,2-rearrangement of differently α,α-disubstituted a-siloxy aldehydes

Ohmatsu, Kohsuke,Tanaka, Takayuki,Ooi, Takashi,Maruoka, Keiji

supporting information; experimental part, p. 5203 - 5206 (2009/04/11)

(Chemical Equation Presented) Control of the migration tendency: The regiodivergent 1,2-rearrangement of asiloxy aldehydes bearing α-aryl and α-alkyl substituents into α-siloxy ketones has been realized by using different aluminum Lewis acid catalyst/solvent systems (see scheme). The scope of this unprecedented protocol has been investigated with various substrates and clearly demonstrates its utility for the selective synthesis of two structural isomers from one substrate.

ENANTIOSELECTIVE SYNTHESIS OF PROTECTED α-HYDROXY ALDEHYDES AND KETONES VIA HYDROXYLATION OF METALATED CHIRAL HYDRAZONES

Enders, Dieter,Bhushan, Vidya

, p. 2437 - 2440 (2007/10/02)

α-Benzyloxy aldehydes and α-acetoxy ketones 4 of high enantiomeric purity are prepared in good overall yields via oxaziridine mediated hydroxylation of chiral hydrazone azaenolates.As auxiliaries novel proline derived hydrazine reagents 5 are used.

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