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α-Carbethoxy-α-diethoxymethyl-β-(3,4,5-trimethoxyphenyl)propionitrile is a complex organic compound with the molecular formula C18H23NO6. It is characterized by a propionitrile group (a three-carbon chain with a nitrile group at one end and a carboxylic acid group at the other), which is substituted with an α-carbethoxy group (an ester of acetic acid) and an α-diethoxymethyl group (a methyl group with two ethoxy groups attached). Additionally, the molecule features a 3,4,5-trimethoxyphenyl group, which is a phenyl ring with three methoxy groups attached at the 3rd, 4th, and 5th positions. α-carbethoxy-α-diethoxymethyl-β-(3,4,5-trimethoxyphenyl)propionitrile 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 specialty chemicals. Its unique structure and functional groups make it a valuable building block in organic synthesis, allowing for the creation of a wide range of derivatives with diverse properties and uses.

65708-35-2

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65708-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65708-35-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 65708-35:
(7*6)+(6*5)+(5*7)+(4*0)+(3*8)+(2*3)+(1*5)=142
142 % 10 = 2
So 65708-35-2 is a valid CAS Registry Number.

65708-35-2Downstream Products

65708-35-2Relevant 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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