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2-(4-chloro-2-fluorophenyl)-2,2-difluoroacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1523486-08-9

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1523486-08-9 Usage

Molecular class

Synthetic organic compound

Type of acid

Difluoroacetic acid

Characteristic functional group

4-chloro-2-fluorophenyl group attached to the difluoroacetic acid moiety

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals, research and development, production of fluorinated compounds with potential biological activity

Handling precautions

May pose a risk to human health and the environment if not properly handled and disposed of.

Check Digit Verification of cas no

The CAS Registry Mumber 1523486-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,3,4,8 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1523486-08:
(9*1)+(8*5)+(7*2)+(6*3)+(5*4)+(4*8)+(3*6)+(2*0)+(1*8)=159
159 % 10 = 9
So 1523486-08-9 is a valid CAS Registry Number.

1523486-08-9Downstream Products

1523486-08-9Relevant academic research and scientific papers

Synthetic method of aromatic ring group or aromatic heterocyclic tetrazole

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Paragraph 0055-0062; 0071, (2020/12/30)

The synthetic method comprises the following steps: (1) reacting 1.0 eq of ArI or HArI with 1.2 eq of ethyl 2, 2-difluoroacetate in the presence of DMSO as a solvent and 4.0 eq of Cu under the protection of nitrogen at 30 DEG C and 50 DEG C, and purifying to obtain a first intermediate compound; (2) dissolving 1.0 eq of the first intermediate compound in a mixed solvent of THF and water, adding 2.0 eq of LiOH, reacting at room temperature for 2 hours, spin-drying the solvent, adding HCl until the pH value is equal to 3, and filtering to obtain a second intermediate compound; and (3) reacting 1.0 eq of the second intermediate compound with 2.0 eq of diphenyl azide phosphate in the presence of 2.5 eq of triethylamine by taking tert-butyl alcohol as a solvent to generate aromatic ring group or aromatic heterocyclic tetrazole. The invention provides a novel synthetic method of aromatic ring group or aromatic heterocyclic tetrazole, wherein a target compound can be more conveniently obtained, and reagents participating in the reaction are low in toxicity, mild in reaction condition, simple and safe in aftertreatment, good in product quality and suitable for large-scale production.

Substituted amide phenol compound and its preparation method, pharmaceutical composition and use thereof

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, (2019/07/04)

The invention discloses substituted-amide phenolic compounds, their preparation method, a pharmaceutical composition and an application thereof. The compounds have a structure as shown in the general formula I, wherein Z, L and Q are as defined in the spe

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