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tert-butyl 4-(4-((4-chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)phenyl)piperidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1383682-52-7

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1383682-52-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383682-52-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,6,8 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1383682-52:
(9*1)+(8*3)+(7*8)+(6*3)+(5*6)+(4*8)+(3*2)+(2*5)+(1*2)=187
187 % 10 = 7
So 1383682-52-7 is a valid CAS Registry Number.

1383682-52-7Downstream Products

1383682-52-7Relevant academic research and scientific papers

FAK AND FLT3 INHIBITORS

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, (2014/03/22)

The use of a compound of the formula (I): (Formula (I)) in the preparation of a medicament for treating Acute Myeloid Leukemia or a disease ameliorated by the inhibition of Flt3, or Flt3 and FAK.

VEGFR3 INHIBITORS

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Page/Page column 87, (2014/03/22)

This invention relates to a compound of the formula (I): The invention also relates to processes for the preparation of the compound of the formula (I), pharmaceutical agents or compositions containing the compound or a method of using the compound for th

VEGFR3 INHIBITORS

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Page/Page column 78; 79, (2014/03/22)

This invention relates to compounds of the formula (I). The invention also relates to processes for the preparation of the compound of the formula (I), pharmaceutical agents or compositions containing the compound or a method of using the compound for the treatment of proliferative diseases, such as cancer as well as the treatment of diseases ameliorated by the control and/or inhibition of lymphanglogenesis.

FAK INHIBITORS

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, (2012/09/10)

A compound of the formula (I): where R1 or R2 is a cycle amine group and R5 is an aromatic group with a carbonyl containing substituent for use as a FAK inhibitor.

OXINDOLOPYRIMIDINE AS IGF1R RECEPTOR INHIBITORS

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Page/Page column 65; 68, (2012/07/13)

The present invention encompasses compounds of general formula (I) wherein the groups R5 to R10, A, L1, B, m and p are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.

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