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2-(3,4-dimethoxy-phenyl)-1,3-propane-diol, also known as 2-(3,4-dimethoxyphenyl)propane-1,3-diol, is a chemical compound with the molecular formula C11H16O4. It is a colorless to pale yellow liquid with a molecular weight of 208.24 g/mol. This organic compound features a propane backbone with two hydroxyl groups at the 1 and 3 positions, and a 3,4-dimethoxyphenyl group attached at the 2 position. The presence of two methoxy groups on the phenyl ring contributes to its lipophilic nature, while the hydroxyl groups provide hydrophilic properties. 2-(3,4-dimethoxy-phenyl)-1,3-propane-diol is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also known for its potential applications in the development of new materials and as a building block in organic synthesis.

717-51-1

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717-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 717-51-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 717-51:
(5*7)+(4*1)+(3*7)+(2*5)+(1*1)=71
71 % 10 = 1
So 717-51-1 is a valid CAS Registry Number.

717-51-1Relevant academic research and scientific papers

Enzymatic desymmetrization of prochiral 2-substituted-1,3-diamines: Preparation of valuable nitrogenated compounds

Rios-Lombardia, Nicolas,Busto, Eduardo,Garcia-Urdiales, Eduardo,Gotor-Fernandez, Vicente,Gotor, Vicente

supporting information; experimental part, p. 2571 - 2574 (2009/07/25)

A wide range of prochiral 1, 3-diamines were first efficiently synthesized and subsequently desymmetrized by using lipase from Pseudomonas cepacia as catalyst and diallyl carbonate as alkoxycarbonylating agent. In all cases, the amino carbamates of R-configuration were recovered. Final selective cleavage of the N-allyloxycarbonyl moiety was carried out under mild reaction conditions, which demonstrates the high versatility and potential of this chemoenzymatic route as a source of intermediates in the synthesis of related optically active nitrogenated derivatives.

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