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5-(Phenylmethyl)quinolin-8-ol is a chemical compound with the molecular formula C20H17NO. It is a derivative of quinolin-8-ol, featuring a phenylmethyl group attached to the 5th position of the quinoline ring. This organic molecule is characterized by its aromatic structure, which includes a quinoline ring system and a benzene ring. It is a white to off-white crystalline solid and is soluble in organic solvents. The compound may have potential applications in the fields of pharmaceuticals and materials science, although specific uses are not detailed here. Its synthesis and properties are of interest to researchers in organic chemistry.

6954-93-4

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6954-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6954-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6954-93:
(6*6)+(5*9)+(4*5)+(3*4)+(2*9)+(1*3)=134
134 % 10 = 4
So 6954-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO/c18-15-9-8-13(11-12-5-2-1-3-6-12)14-7-4-10-17-16(14)15/h1-10,18H,11H2

6954-93-4Downstream Products

6954-93-4Relevant academic research and scientific papers

IDO inhibitors

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, (2018/09/02)

Presently provided are methods for (a) modulating an activity of indoleamine 2,3-dioxygenase comprising contacting an indoleamine 2,3-dioxygenase with a modulation effective amount of a compound as described in one of the aspects described herein; (b) treating indoleamine 2,3-dioxygenase (IDO) mediated immunosuppression in a subject in need thereof, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (c) treating a medical conditions that benefit from the inhibition of enzymatic activity of indoleamine-2,3-dioxygenase comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; (d) enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent and a compound as described in one of the aspects described herein; (e) treating tumor-specific immunosuppression associated with cancer comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount of a compound as described in one of the aspects described herein; and (f) treating immunosuppression associated with an infectious disease, e.g., HIV-I infection, comprising administering an effective indoleamine 2,3-dioxygenase inhibiting amount a compound as described in one of the aspects described herein.

1,2,3,4-tetrahydro-8-quinolinol derivatives and anti-allergic use thereof

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, (2008/06/13)

Leukotriene biosynthesis in macrophage cells is inhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof, wherein R1 and R2 are each hydrogen and R3 is alkyl or arylalkyl; R1

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