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1246560-12-2

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1246560-12-2 Usage

Type of Compound

Ketone

Structure

Substituted phenyl group and a boron-containing moiety

Applications

a. Organic synthesis
b. Building block in pharmaceuticals and agrochemicals development
c. Reagent in Suzuki coupling reactions and other organic transformations
d. Ligand in coordination chemistry and catalysis

Unique Features

a. Boron-containing group
b. Valuable for a variety of applications
c. Interest to researchers and industries in complex organic molecule synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 1246560-12-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,5,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1246560-12:
(9*1)+(8*2)+(7*4)+(6*6)+(5*5)+(4*6)+(3*0)+(2*1)+(1*2)=142
142 % 10 = 2
So 1246560-12-2 is a valid CAS Registry Number.

1246560-12-2Downstream Products

1246560-12-2Relevant articles and documents

SUBSTITUTED PYRAZOLOPYRIMIDINES AND SUBSTITUTED PURINES AND THEIR USE AS UBIQUITIN-SPECIFIC-PROCESSING PROTEASE 1 (USP1) INHIBITORS

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Paragraph 0723, (2020/07/14)

The present disclosure provides compounds having Formula I: and the pharmaceutically acceptable salts and solvates thereof, wherein X1, X2, X11, X12, R1, R3, R5, R5', R6, and R7 are defined as set forth in the specification. The present disclosure is also directed to the use of compounds of Formula I to inhibit a USP1 protein and/or to treat a disorder responsive to the inhibition of USP1 proteins and USP1 activity. Compounds of the present disclosure are especially useful for treating cancer.

Palladium-catalyzed borylation of aryl mesylates and tosylates and their applications in one-pot sequential suzuki-miyaura biaryl synthesis

Chow, Wing Kin,So, Chau Ming,Lau, Chak Po,Kwong, Fuk Yee

, p. 6913 - 6917 (2011/08/03)

Top of the one-pots! The first palladium-catalyzed borylation of aryl tosylates and mesylates is described. The reaction conditions are mild and provide excellent functional-group compatibility (e.g., R=CN, CHO, COOMe, C(O)R, NH2, or NH-indole; see scheme). Pd/MeO-CM-phos allows one-pot sequential reactions in the preparation of unsymmetrical biaryls. Copyright

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