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

145348-99-8

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145348-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145348-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,4 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145348-99:
(8*1)+(7*4)+(6*5)+(5*3)+(4*4)+(3*8)+(2*9)+(1*9)=148
148 % 10 = 8
So 145348-99-8 is a valid CAS Registry Number.

145348-99-8Relevant academic research and scientific papers

2 - (5 - fluoro - 2, 4 - II nitrobenzene oxygen) acetate synthesis method

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Paragraph 0032, (2017/08/26)

The invention belongs to the field of chemical sythensis, and particularly relates to a synthetic method of 2-(5-fluoro-2,4-nitrophenoxy)acetate. The invention aims to solve the technical problem that the separation and purification of a product is difficult, and the production cost is high. For solving the technical problem, the synthetic method of 2-(5-fluoro-2,4-nitrophenoxy)acetate is provided. The synthetic method comprises the following steps: a, reacting 2,4-difluoronitrobenzene with glycolate under the action of an acid-binding agent so as to obtain a mixture of 2-(5-fluoro-2-nitrophenoxy)acetate and 2-(3-fluoro-4-nitrophenoxy)acetate; b, reacting the mixture obtained in the step a with nitric acid to obtain 2-(5-fluoro-2,4-dinitrophenoxy)acetate. According to the synthetic method, raw materials are cheap and easily available, reaction selectivity is good, side reaction is less, product yield in high, reaction condition is mild and easy to control, and process is simple to operate and easy to industrialize.

Benzoxazepinones and their use as squalene synthase inhibitors

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, (2008/06/13)

There is disclosed a compound represented by the formula [I]: wherein R1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, -X1-X2-Ar-X3-X4-COOH (wherein X1 and X4 are a bond or alkylene group, X2 and X3 are a bond, -O-, -S-, Ar is divalent aromatic group etc.), R2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.

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