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(R)-2-(((R)-2-hydroxy-1-phenylethyl) amino)-2-(trifluoromethyl)hexan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1352790-08-9

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1352790-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352790-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,7,9 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1352790-08:
(9*1)+(8*3)+(7*5)+(6*2)+(5*7)+(4*9)+(3*0)+(2*0)+(1*8)=159
159 % 10 = 9
So 1352790-08-9 is a valid CAS Registry Number.

1352790-08-9Relevant academic research and scientific papers

COMBINATION OF HEPATITIS B VIRUS (HBV) VACCINES AND PYRIDOPYRIMIDINE DERIVATIVES

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Page/Page column 365; 366, (2021/01/22)

Therapeutic combinations of hepatitis B virus (HBV) vaccines and a pyridopyrimidine derivative are described. Methods of inducing an immune response against HBV or treating an HBV-induced disease, particularly in individuals having chronic HBV infection, using the disclosed therapeutic combinations are also described. The invention provides therapeutic combinations or compositions and methods for inducing an immune response against hepatitis B viruses (HBV) infection.

TOLL LIKE RECEPTOR MODULATOR COMPOUNDS

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Paragraph 0956; 0959, (2016/10/27)

The present disclosure relates generally to toll like receptor modulator compounds, such as diamino pyrido[3,2 D]pyrimidine compounds and pharmaceutical compositions which, among other things, modulate toll-like receptors (e.g. TLR-8), and methods of making and using them.

Highly diastereoselective synthesis of enantiopure β-trifluoromethyl β-amino alcohols from chiral trifluoromethyl oxazolidines (Fox)

Simon, Julien,Chelain, Evelyne,Brigaud, Thierry

supporting information; experimental part, p. 604 - 607 (2012/03/10)

The organolithium species addition to 2-hydroxymethyl fluorinated oxazolidines (Fox) provides a highly diastereoselective and straightforward route for the synthesis of enantiopure trifluoromethyl β-amino alcohols quaternarized at the β-position.

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