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methyl 3-nitro-4-(2-oxopropyl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

206066-05-9

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206066-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206066-05-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,0,6 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 206066-05:
(8*2)+(7*0)+(6*6)+(5*0)+(4*6)+(3*6)+(2*0)+(1*5)=99
99 % 10 = 9
So 206066-05-9 is a valid CAS Registry Number.

206066-05-9Downstream Products

206066-05-9Relevant academic research and scientific papers

RING-FUSED COMPOUND

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, (2014/01/07)

The present invention relates to a compound that has URAT1 inhibitory action, and a URAT1 inhibitor, a blood uric acid level-reducing agent and a pharmaceutical composition comprising the compound. More specifically, the present invention relates to a compound represented by Formula (I) below. [in the formula, R1 is -Q1-A1 and the like; ---- is a double bond or a single bond; when ---- is a double bond, W1 is a nitrogen atom or a group represented by the general formula: =C(Ra)-, and W2 is a nitrogen atom or a group represented by the general formula: =C(Rb) -; when ---- is a single bond, W1 is a group represented by the general formula: -C(Raa)(Rab)- or a group represented by the general formula: -(C=O) -, and W2 is a group represented by the general formula: C(Rba)(Rbb)-, a group represented by the general formula: - (C=O) - or a group represented by the general formula: -N(Rbc)-; W3, W4 and W5 are each independently a nitrogen atom or a methine group and the like that may have a substituent; X is a single bond, an oxygen atom and the like; Y is a single bond or (CRYiRYi')n; and Z is a hydroxyl group or COOR2 and the like.

Method for inhibiting neoplastic cells with indole derivatives

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, (2008/06/13)

A method for inhibiting neoplastic cells and related conditions by exposing them to substituted indole derivatives.

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