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1,3-Dioxane-4,6-dione, 5-[[[4-(acetyloxy)-3-methoxyphenyl]amino]methylene]-2,2-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

205448-73-3

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205448-73-3 Usage

Chemical structure

A complex chemical compound with a dioxane ring and a methylene group.

Functional groups

Contains an acetyloxy group and a methoxyphenyl group.

Unique structure

The combination of the dioxane ring, methylene group, acetyloxy group, and methoxyphenyl group gives 1,3-Dioxane-4,6-dione, 5-[[[4-(acetyloxy)-3-methoxyphenyl]amino]methylene]-2,2-dimethyl- a unique structure.

Potential medicinal properties

It may have potential medicinal properties and could be used in pharmaceutical research or manufacturing.

Precaution

It is important to handle and use this chemical with caution, as its precise properties and potential effects on health and the environment may require further study.
Please note that this list is based on the limited information provided in the material and may not be exhaustive. Further research and study may be necessary to fully understand the properties and potential applications of 1,3-Dioxane-4,6-dione, 5-[[[4-(acetyloxy)-3-methoxyphenyl]amino]methylene]-2,2-dimethyl-.

Check Digit Verification of cas no

The CAS Registry Mumber 205448-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,4,4 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 205448-73:
(8*2)+(7*0)+(6*5)+(5*4)+(4*4)+(3*8)+(2*7)+(1*3)=123
123 % 10 = 3
So 205448-73-3 is a valid CAS Registry Number.

205448-73-3Relevant academic research and scientific papers

QUINOLINE AND QUINOXALINE DERIVATIVES AS INHIBITORS OF KINASE ENZYMATIC ACTIVITY

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Page/Page column 79; 81, (2008/06/13)

Compounds of formula (IA) or (IB), are inhibitors of aurora kinase activity: Formula (IA), (IB) wherein -L1Y1-[CH2]z- is a linker radical wherein Y1, L1 and z are as defined in the claims; R6 is C1-C4alkoxy, hydrogen or halo; W represents a bond, -CH2-, -O-, -S-, -S(=O)2-, or -NR5- where R5 is hydrogen or C1-C4 alkyl; Q is =N-, =CH- or =C(X1)- wherein X1 is cyano, cyclopropyl or halo; linker radicals L2 are as defined in the claims; R is a radical of formula (X) or (Y): wherein R1 is a carboxylic acid group (-COOH), or an ester group which is hydrolysable by one or more intracellular carboxylesterase enzymes to a carboxylic acid group; R4 is hydrogen; or optionally substituted C1-C6 alkyl, C3-C7 cycloalkyl, aryl, aryl(C1-C6 alkyl)-, heteroaryl, heteroaryl(C1-C6 alkyl)-, -(C=O)R3, -(C=O)OR3, or -(C=O)NR3 wherein R3 is hydrogen or optionally substituted (C1-C6)alkyl, C3-C7 cycloalkyl, aryl, aryl(C1-C6 alkyl)-, heteroaryl, or heteroaryl(C1-C6 alkyl)-; R41 is hydrogen or optionally substituted C1-C6 alkyl; and D is a monocyclic heterocyclic ring of 5 or 6 ring atoms.

Quinoline derivatives inhibiting the effect of growth factors such as VEGF

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Page column 71, (2010/02/08)

Compounds of the formula (I): wherein: R2represents hydroxy, halogeno, C1-3alkyl, C1-3alkoxy, C1-3alkanoyloxy, trifluoromethyl, cyano, amino or nitro; n is an integer from 0 to 5; Z represents —O—, —NH—, —S— or —CH2—; G1represents phenyl or a 5-10 membered heteroaromatic cyclic or bicyclic group; Y1, Y2, Y3and Y4each independently represents carbon or nitrogen; R1represents fluoro or hydrogen; m is an integer from 1 to 3; R3represents hydrogen, hydroxy, halogeno, cyano, nitro, trifluoromethyl, C1-3alkyl, —NR4R5(wherein R4and R5, can each be hydrogen or C1-3alkyl), or a group R6—X1— wherein X1represents —CH2— or a heteroatom linker group and R6is an alkyl, alkenyl or alkynyl chain optionally substituted by for example hydroxy, amino, nitro, alkyl, cycloalkyl, alkoxyalkyl, or an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring, which alkyl, alkenyl or alkynyl chain may have a heteroatom linker group, or R6is an optionally substituted group selected from pyridone, phenyl and a heterocyclic ring and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals such as humans, processes for the preparation of such derivatives, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula I. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.

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