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Methoxy(thiophen-2-yl)acetic acid is an organic compound with the chemical formula C6H7O3S. It is a derivative of acetic acid, featuring a methoxy group (-OCH3) and a thiophene ring (a five-membered aromatic ring containing sulfur) attached to the acetic acid backbone. methoxy(thiophen-2-yl)acetic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of certain specialty chemicals. Its unique structure, which combines the properties of both aromatic and sulfur-containing compounds, makes it an interesting molecule for researchers in the field of organic chemistry.

5371-94-8

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5371-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5371-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5371-94:
(6*5)+(5*3)+(4*7)+(3*1)+(2*9)+(1*4)=98
98 % 10 = 8
So 5371-94-8 is a valid CAS Registry Number.

5371-94-8Downstream Products

5371-94-8Relevant academic research and scientific papers

Preparation method of (RS)-methoxy cefoxitin

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Paragraph 0042-0051, (2019/10/01)

The invention discloses a preparation method of (RS)-methoxy cefoxitin, which is characterized by comprising the following steps: (1) taking thiophene as an initial raw material, n-heptane as a reaction solvent, reacting with trichloroacetaldehyde, and distilling under reduced pressure after the reaction; (2) reacting the product of the step (1) with methanol in the presence of alkaline substancesto prepare (RS)-alpha-methoxy-2-thiophenephenylacetic acid; (3) dissolving the (RS)-alpha-methoxy-2-thiophenephenylacetic acid in an organic solvent, adding a first organic base, stirring and clarifying, and dripping methanesulfonyl chloride or pivaloyl chloride for later use; adding HACA and an organic solvent into another reaction vessel, adding a second organic base, and stirring the mixture until the mixture is clarified for later use; slowly dripping a solution B into a solution A at below -30 DEG C; then dropwise adding chlorosulfonyl isocyanate to react to obtain white-like crystallinepowder; and (4) reacting the white-like crystalline powder with sodium methoxide to obtain a product. The purity of the product is high.

SUBSTITUTED DIHYDROPYRROLOPYRAZOLE COMPOUND

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Paragraph 1001-1003, (2017/09/12)

Provided is a compound represented by formula (I) or a pharmacologically acceptable salt thereof: wherein L1 is an optionally substituted C1-6 alkylene group or the like, L2 is a single bond or the like, L3 is a single bond or the like, R1, R2, and R3 are each independently an optionally substituted C1-4 alkyl group or the like, R4 is a hydrogen atom or the like, and R5 is a hydrogen atom or the like.

Process for preparing thiophene derivatives and thiophene derivatives obtained thereby

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, (2008/06/13)

Process for the preparation of a series of thiophene derivatives, from which 2-thiopheneacetic acid derivatives can easily be prepared, in high yields and selectivity by using substituted or unsubstituted thiophenes as the starting materials by easy operations. 2-Thiopheneacetic acid derivatives are very useful compounds as the chemical modifier of penicillin and cephalosporin. Novel compounds, i.e. α-arylthio-2-thiopheneacetic acids are also disclosed. These compounds are useful as the intermediates of the synthesis of 2-thiopheneacetic acids.

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