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(R,Z)-4-hydroxy-N,N-diphenylpent-2-enamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

900160-96-5

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900160-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 900160-96-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,1,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 900160-96:
(8*9)+(7*0)+(6*0)+(5*1)+(4*6)+(3*0)+(2*9)+(1*6)=125
125 % 10 = 5
So 900160-96-5 is a valid CAS Registry Number.

900160-96-5Downstream Products

900160-96-5Relevant academic research and scientific papers

7A-HETEROCYCLE SUBSTITUTED- 6, 6-DIFLUORO BICYCLIC HIMBACINE DERIVATIVES

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Page/Page column 23; 24; 25, (2015/03/13)

The present invention relates to bicyclic himbacine derivatives of the formula, stnjctrually represented, or a pharmaceutically acceptable salt thereof wherein: R1 is any of the recited compounds, W is any of the recited compounds and the remaining variab

7A-AMIDE SUBSTITUTED-6,6-DIFLUORO BICYCLIC HIMBACINE DERIVATIVES

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Page/Page column 22; 23; 24, (2015/03/13)

The present invention relates to bicyclic himbacine derivatives of the formula (structurally represented) or a pharmaceutically acceptable salt thereof wherein: R1 is -[C(Ra)(Rb)]x-[C(Rb)(Rb)]y-C(0)NH2, or -N(H)-[(CH2)]zC(0)-NH2; W is any of the recited c

3'-PYRIDYL SUBSTITUTED- 6,6-DIFLUORO BICYCLIC HIMBACINE DERIVATIVES

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Page/Page column 23, (2015/03/13)

The present invention relates to bicyclic himbacine derivatives of the formula or a pharmaceutically acceptable salt thereof wherein: R1 is halo; -CN; alkyi; cycloalkyi; alkoxy; phenyl, which is optionally substituted one or twice independently by alkyi,

AN EXO-SELECTIVE SYNTHESIS OF HIMBACINE ANALOGS

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Page/Page column 30-32, (2008/06/13)

This application discloses a novel process for the synthesis of himbacine analogs, as well as the compounds produced thereby. The synthesis proceeds by alternative routes including the cyclic ketal amide route, the chiral carbamate amide route, and the ch

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