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α-Carbethoxy-α-diethoxymethyl-β-[3,4-dimethoxyphenyl]propionitrile is a complex organic compound with the molecular formula C16H21NO5. It features a propionitrile group (a nitrile-containing propionic acid derivative), a carbethoxy group (an ester of carboxylic acid), and a diethoxymethyl group. The molecule also contains a 3,4-dimethoxyphenyl ring, which is a phenyl ring with two methoxy groups attached at the 3rd and 4th carbon positions. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and other bioactive compounds. Its structure and properties make it a versatile building block in organic synthesis, allowing for the creation of a wide range of molecules with different biological activities.

65708-36-3

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65708-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65708-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65708-36:
(7*6)+(6*5)+(5*7)+(4*0)+(3*8)+(2*3)+(1*6)=143
143 % 10 = 3
So 65708-36-3 is a valid CAS Registry Number.

65708-36-3Downstream Products

65708-36-3Relevant academic research and scientific papers

Benzyl cyanoacetals

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, (2008/06/13)

Benzyl cyanoacetals of formula: STR1 wherein R1, R2 and R3 are the same or different and each is a halogen or a hydrogen atom, an alkoxy group, an alkyl group, or a dialkylamino group; R4 is an alkoxycarbonyl group, or an aldehyde group; And R5 is an alkyl group; the alkyl or alkoxy groups each having from 1 to 4 carbon atoms, and their use as intermediates in the preparation of antibacterial 2,4-diamino-5-benzylpyrimidines. They are prepared from a reaction between an orthoester and an α-substituted-β-benzylpropionitrile and then the resulting cyanoacetal is converted to the benzyl-pyrimidine by reaction with guanidine.

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