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(+/-)-3-Diaethylamino-1-phenyl-butan-1-on, also known as 3-(diethylamino)-1-phenylbutan-1-one, is an organic compound with the molecular formula C14H21NO. It is a chiral molecule, meaning it has two enantiomeric forms, (+) and (-), which are mirror images of each other. (+/-)-3-Diaethylamino-1-phenyl-butan-1-on is a derivative of 1-phenylbutan-1-one, with a diethylamino group (-N(C2H5)2) attached to the 3rd carbon. It is a colorless to pale yellow liquid with a characteristic amine-like odor. (+/-)-3-Diaethylamino-1-phenyl-butan-1-on is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its chiral nature makes it an important compound in the field of asymmetric synthesis, where the development of enantioselective methods for its preparation is of great interest.

3506-61-4

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3506-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3506-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3506-61:
(6*3)+(5*5)+(4*0)+(3*6)+(2*6)+(1*1)=74
74 % 10 = 4
So 3506-61-4 is a valid CAS Registry Number.

3506-61-4Downstream Products

3506-61-4Relevant academic research and scientific papers

Alkoxide activation of aminoboranes towards selective amination

Sole, Cristina,Fernandez, Elena

, p. 11351 - 11355 (2013)

Piece of the (inter)action: The interaction of alkoxides with the sp 2 Bpin (pin=pinacol) moiety in aminoboranes forms the in situ Lewis acid-base adduct [RO-→B(OR)2-N(R′)2] which enables the amino moiety to react as a strong nucleophile with several electrophiles, thus providing amino alcohols, β-enamino esters, and β-hydroxy amides in a direct and remarkably selective way (see scheme). Copyright

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