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76352-71-1

Benzenepropanoic acid, a-ethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76352-71-1 Structure

  • Basic information

    1. Product Name: Benzenepropanoic acid, a-ethyl-, methyl ester
    2. Synonyms:
    3. CAS NO:76352-71-1
    4. Molecular Formula: C12H16O2
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76352-71-1.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: Benzenepropanoic acid, a-ethyl-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepropanoic acid, a-ethyl-, methyl ester(76352-71-1)
    11. EPA Substance Registry System: Benzenepropanoic acid, a-ethyl-, methyl ester(76352-71-1)

  • 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: 76352-71-1(Hazardous Substances Data)

76352-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76352-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,5 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76352-71:
(7*7)+(6*6)+(5*3)+(4*5)+(3*2)+(2*7)+(1*1)=141
141 % 10 = 1
So 76352-71-1 is a valid CAS Registry Number.

76352-71-1Relevant articles and documents

NEW METHOD FOR GENERATION OF THIOCARBONYL YLIDES FROM BIS(TRIMETHYLSILYLMETHYL)SULFOXIDES AND THEIR APPLICATION TO CYCLOADDITIONS

Aono, Masaaki,Terao, Yoshiyasu,Achiwa, Kazuo

, p. 249 - 260 (2007/10/02)

Thiocarbonyl ylides were generated by heating of bis(trimethylsilylmethyl)sulfoxides.Cycloadditions of the ylides in the presence of dipolarophiles proceeded smoothly to give di- or tetrahydrothiophenes.

CHEMOENZYMATIC SYNTHESIS OF THE ENANTIOMERS OF IOPANOIC ACID

Colombo, M.,Amici, M. De,Micheli, C. De,Pitre, D.,Carrea, G.,Riva, S.

, p. 1021 - 1030 (2007/10/02)

The two enantiomers of Iopanoic acid 1 were prepared in enantiomeric excess higher than 90percent by enzyme-catalyzed hydrolysis of precursors (+/-)-2a and (+/-)-3a, followed by standard chemical transformations.Among the tested enzymes, chymotrypsin and Lipase PS proved to be the most selective catalysts.The stereochemical outcome of the lipase-catalyzed hydrolyses of esters (+/-)-2a-d is strictly dependent upon both the size of the alkyl group attached to the chiral center and the substituent in the aromatic ring.The enantioselectivity of the reactions was evaluated by chiral HPLC and the configurations of the new products were assigned by chemical correlations.

Synthesis of 3-Phenoxybenzyl 3-Alkyl-3-phenyl-/p-substituted phenyl and 3-Phenoxybenzyl 2-Alkyl-3-phenyl-/p-substituted phenylpropionates

Kelkar, S. V.,Joshi, G. S.,Kulkarni, G. H.,Mitra, R. B.

, p. 68 - 70 (2007/10/02)

Some 3-phenoxybenzyl 3-alkyl-3-phenyl-/p-substituted phenylpropionates (VII, XI, XV, XIX, XXIII, XXVII) which resemble structurally the 1,2-secopyrethroids, have been prepared employing simple reactions like alkylation, decarbethoxylation and transesterification.The synthesis of 3-phenoxybenzyl 2-alkyl-3-phenyl-/p-substituted phenyl-propionates (XXXI, XXXII, XXXIII, and XXXVI) bearing close structural resemblance to 2,3-secopyrethroids has also been described.

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