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Cyclohexanone, 2-(1,1-dimethylethyl)-, (2R)-, also known as (2R)-2-tert-amylcyclohexanone, is a chiral ketone with the molecular formula C10H18O. It is a colorless liquid with a molecular weight of 154.25 g/mol. Cyclohexanone, 2-(1,1-dimethylethyl)-, (2R)- is characterized by its cyclohexanone core, which features a six-membered carbon ring with a ketone group (C=O) at the 2-position. The 1,1-dimethylethyl (tert-amyl) group is attached to the 2-position, giving the molecule its unique structure. The (2R)- configuration indicates that the molecule has a specific arrangement of atoms in three-dimensional space, which is important in understanding its stereochemistry. Cyclohexanone, 2-(1,1-dimethylethyl)-, (2R)- is used in the synthesis of various chemicals and pharmaceuticals, and its properties, such as solubility and reactivity, are influenced by its stereochemistry.

3763-51-7

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3763-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3763-51-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3763-51:
(6*3)+(5*7)+(4*6)+(3*3)+(2*5)+(1*1)=97
97 % 10 = 7
So 3763-51-7 is a valid CAS Registry Number.

3763-51-7Downstream Products

3763-51-7Relevant academic research and scientific papers

Secondary Phosphine Oxides as Multitalented Preligands En Route to the Chemoselective Palladium-Catalyzed Oxidation of Alcohols

Vasseur, Alexandre,Membrat, Romain,Gatineau, David,Tenaglia, Alphonse,Nuel, Didier,Giordano, Laurent

, p. 728 - 732 (2017/03/13)

Secondary phosphine oxides O=PHR2 (SPOs) were identified as multitalented preligands for the chemoselective Pd-catalyzed oxidation of alcohols by a hydrogen-abstracting methodology. SPOs were found to promote the hydrogen-abstraction step as well as hydrogen transfer to a Michael acceptor by generating a putative active H?Pd species. The catalytic system operates under neutral conditions and was proven to be compatible with various electrophilic and nucleophilic functionalities within the substrates as well as water- and air-sensitive functional groups.

N,S-DIMETHYL-S-PHENYLSULFOXIMINE. A REAGENT FOR THE OPTICAL RESOLUTION OF KETONES

Johnson, Carl R.,Zeller, James R.

, p. 1225 - 1234 (2007/10/02)

The addition of the α-lithio derivative of (+)- or (-)-N,S-dimethyl-S-phenylsulfoximine to selected dl-ketones was carried out at -78 deg C in tetrahydrofuran followed by acid quench at that temperature to produce mixtures of diastereomeric β-hydroxysulfoximines.The optically-active diastereomers were chromatographically separated on silica gel.The purified diastereomers were thermolyzed at ca. 130 deg to produce optically-active ketones and the optically-active sulfoximine which could be recycled.

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