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7-chloro-5-methoxyquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1935618-88-4

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1935618-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1935618-88-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,3,5,6,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1935618-88:
(9*1)+(8*9)+(7*3)+(6*5)+(5*6)+(4*1)+(3*8)+(2*8)+(1*8)=214
214 % 10 = 4
So 1935618-88-4 is a valid CAS Registry Number.

1935618-88-4Downstream Products

1935618-88-4Relevant academic research and scientific papers

COMBINATION PRODUCT FOR THE TREATMENT OF CANCEROUS DISEASES

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Page/Page column 125, (2021/12/31)

The present invention relates to a product for combination therapies useful for the treatment of cancer diseases. In particular, the invention relates to the combination of an anti-PD-Ll antibody and an MCT4 inhibitor of Formula (I). The therapeutic combination may be utilized for the use in treating a subject having a cancer disease that tests positive for PD-L1 and/or MCT4 expression.

DISUBSTITUTED ALKYNE DERIVATIVES

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Page/Page column 119, (2020/07/14)

The present invention relates to disubstituted alkyne derivatives. These compounds are useful for the prevention and/or treatment of several medical conditions including hyperproliferative disorders and diseases.

Synthesis of 5-hydroxyquinolines

Li, Jianke,Kung, Daniel W.,Griffith, David A.

scheme or table, p. 3876 - 3878 (2010/08/19)

A series of 5-hydroxyquinolines has been prepared via the Skraup reaction. Several regioisomers were made either by selective displacement of a leaving group or by using a bromo substituent as a blocking group. The bromo group was found to be an excellent blocking group due to its stability during the Skraup reaction and easy removal thereafter. Halides at the 5-position of quinoline were found to be much more reactive than those at the 7- and 8-positions. Finally, we have also found a unique method to reduce the pyridyl ring on quinolines, leaving a halogen substituent untouched.

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