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6-methoxy-4-phenyl-3,4-dihydronaphthalen-1(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

368883-84-5

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368883-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 368883-84-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,8,8,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 368883-84:
(8*3)+(7*6)+(6*8)+(5*8)+(4*8)+(3*3)+(2*8)+(1*4)=215
215 % 10 = 5
So 368883-84-5 is a valid CAS Registry Number.

368883-84-5Downstream Products

368883-84-5Relevant academic research and scientific papers

Visible Light Driven and Copper-Catalyzed C(sp3)-H Functionalization of O-Pentafluorobenzoyl Ketone Oximes

Wu, Danhua,Cui, Shuang-Shuang,Bian, Fengling,Yu, Wei

supporting information, p. 6057 - 6061 (2021/08/03)

The C(sp3)-H functionalization of O-pentafluorobenzoyl ketone oximes was implemented under visible light irradiation with copper complexes as catalysts. The reactions involve iminyl-radical-mediated intramolecular hydrogen atom transfer as the key step, w

Exploring the synthetic potential of a marine transaminase including discrimination at a remote stereocentre

Schwarz, Maria,Murphy, Edel J.,Foley, Aoife M.,Woods, David F.,Castilla, Ignacio Abreu,Reen, F. Jerry,Collins, Stuart G.,O'gara, Fergal,Maguire, Anita R.

, p. 188 - 198 (2021/01/18)

The marine transaminase, P-ω-TA, can be employed for the transamination from 1-aminotetralins and 1-aminoindanes with differentiation of stereochemistry at both the site of reaction and at a remote stereocentre resulting in formation of ketone products with up to 93% ee. While 4-substituents are tolerated on the tetralin core, the presence of 3- or 8-substituents is not tolerated by the transaminase. In general P-ω-TA shows capacity for remote diastereoselectivity, although both the stereoselectivity and efficiency are dependent on the specific substrate structure. Optimum efficiency and selectivity are seen with 4-haloaryl-1-aminotetralins and 3-haloaryl-1-aminoindanes, which may be associated with the marine origin of this enzyme. This journal is

5- substituted tetralones as inhibitors of ras farnesyl trransferase

-

, (2008/06/13)

The present invention provides novel 5-substituted tetralones of Formulas (I), (II), (III) and (IV) and pharmaceutically acceptable salts, esters, amides, and prodrugs thereof, which are useful for treating and preventing uncontrolled or abnormal proliferation of tissues, such as cancer, atherosclerosis, restenosis, and psoriasis. Specifically, the present invention relates to compounds that inhibit the farnesyl transferase enzyme.

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