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1-acetoxy-1-(3,4-dimethoxy-phenyl)-acetone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38007-20-4

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38007-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38007-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,0 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38007-20:
(7*3)+(6*8)+(5*0)+(4*0)+(3*7)+(2*2)+(1*0)=94
94 % 10 = 4
So 38007-20-4 is a valid CAS Registry Number.

38007-20-4Relevant academic research and scientific papers

DFRC Method for Lignin Analysis. 1. New Method for β-Aryl Ether Cleavage: Lignin Model Studies

Lu, Fachuang,Ralph, John

, p. 4655 - 4660 (2007/10/03)

A new method for selective and efficient cleavage of arylglycerol-β-aryl (β-O-4) ether linkages in lignins is described and applied to several lignin β-ether models. The term "DFRC" was coined for derivatization followed by reductive cleavage. Derivatization, accompanied by cell wall solubilization, is accomplished with acetyl bromide (AcBr); reductive cleavage of resulting β-bromo ethers utilizes zinc in acetic acid. Degradation monomers, 4-acetoxycinnamyl acetates, from β-ether cleavage by the DFRC method were identified by NMR, GC-MS, and comparison of GC retention times with authentic compounds. Under the conditions used in this study, the β-ether linkage of all models was cleaved in very high (>92%) yield. The DFRC method produces simpler mixtures of monomers with higher yields than alternative hydrolytic methods. Because of its relative simplicity, mild conditions, and exceptional selectivity, this method should become a powerful analytical method for lignin characterization.

Total synthesis of (±)-porosin, a neolignan from Ocotea porosa and Urbanodendron verrucosum (Lauraceae)

Matsumoto,Takeda,Oiwamoto,Fujii,Kishida,Shibutani,Imai

, p. 2099 - 2104 (2007/10/03)

Veratraldehyde was condensed with methyl 2-chloropropanoate to give a glycidic ester. This was hydrolyzed with aqueous sodium hydroxide and the resulting sodium salt was treated with lead(IV) tetraacetate to give 1- acetoxy-1-(3,4-dimethoxyphenyl)propon-2

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