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139600-93-4

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139600-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139600-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,0 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139600-93:
(8*1)+(7*3)+(6*9)+(5*6)+(4*0)+(3*0)+(2*9)+(1*3)=134
134 % 10 = 4
So 139600-93-4 is a valid CAS Registry Number.

139600-93-4Relevant articles and documents

Dye, colored resin composition, a color filter, and an organic EL display device, a liquid crystal display device

-

, (2016/10/09)

PROBLEM TO BE SOLVED: To provide a colored resin composition that obtains a color filter for satisfying both of heat resistance and solvent resistance, a color filter formed by using the colored resin composition, a high-quality liquid crystal display device and an organic EL display device. SOLUTION: The dye contains a compound represented by formula (I), Z-A+(wherein Z-is a disulfonyl imide anion; A+is a cationic dye; at least any one of Z-and A+has a crosslinkable group). COPYRIGHT: (C)2013,JPOandINPIT

Organocatalyzed enantioselective fluorocyclizations

Lozano, Oscar,Blessley, George,Martinez Del Campo, Teresa,Thompson, Amber L.,Giuffredi, Guy T.,Bettati, Michela,Walker, Matthew,Borman, Richard,Gouverneur, Veronique

supporting information; experimental part, p. 8105 - 8109 (2011/10/03)

Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral indoles (see scheme; Ts=tosyl, Bn=benzyl, Boc=tert-butoxycarbonyl). More than twenty examples for this cascade fluorination-cyclization, which is catalyzed by cinchona alkaloids and employs N-fluorobenzenesulfonimide as the electrophilic fluorine source have been explored, and an unprecedented catalytic asymmetric difluorocyclization has also been identified.

Novel indole α-methylene-γ-lactones as potent inhibitors for AKT-mTOR signaling pathway kinases

Ding, Huasheng,Zhang, Chao,Wu, Xihan,Yang, Chunhao,Zhang, Xiongwen,Ding, Jian,Xie, Yuyuan

, p. 4799 - 4802 (2007/10/03)

In an effort to generate novel anticancer agents, a series of hybrids of α-methylene-γ-lactones and 2-phenyl indoles has been synthesized and evaluated for inhibition activities on the phosphorylation of AKT, mTOR, p70S6 kinase, and 4E-BP1. The results in

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