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α-Methoxy cinnamic acid, also known as 3-methoxycinnamic acid, is an organic compound with the chemical formula C10H10O3. It is a derivative of cinnamic acid, featuring a methoxy group (-OCH3) attached to the alpha carbon, which is the carbon adjacent to the carboxylic acid group. α-methoxy cinnamic acid is a white crystalline solid and is soluble in organic solvents. α-Methoxy cinnamic acid is used in the synthesis of various pharmaceuticals, fragrances, and other organic compounds due to its versatile chemical structure. It is also found in some natural products and has been studied for its potential biological activities, such as antioxidant properties.

90843-50-8

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90843-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90843-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,4 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90843-50:
(7*9)+(6*0)+(5*8)+(4*4)+(3*3)+(2*5)+(1*0)=138
138 % 10 = 8
So 90843-50-8 is a valid CAS Registry Number.

90843-50-8Relevant academic research and scientific papers

Synthesis of the Natural Product Iotrochamide B

Wang,Zhao,Que

, p. 499 - 501 (2019/07/02)

Iotrochamide B is the first cinnamoyl amino acid reported from the marine sponge Iotrochota sp. The total synthesis of the marine indole alkaloid iotrochamide B was achieved by condensation of 6-bromo-L-tryptophan (3) and (Z)-2-methoxy-3-phenylacrylic acid (6). The key step was the synthesis of 6-bromo-L-tryptophan ((S)-3) from racemic N-acetyltryptophan by optical resolution using (S)-(–)-1-phenylethylamine. This work provides an efficient method for future synthesis of iotrochamide B derivatives.

Synthesis of novel cinnamanilides as potential immunosuppressive agents

Shi, Lei,Wang, Lu,Wang, Zhi,Zhu, Hai-Liang,Song, Qiao

, p. 585 - 593 (2012/02/14)

A series of new cinnamanilides (6-40) were synthesized and their immunosuppressive activity and cytotoxicity were evaluated. Most of the cinnamanilides showed good immunosuppressive activity. Among the synthesized compounds, (Z)-N-(4-bromophenyl)-2-methox

Stereoselective addition of 2-aminothiophenol to α-alkoxycinnamic acid derivatives - Alternative synthesis of (±)-diltiazem

Miyata, Okiko,Shinada, Tetsuro,Naito, Takeaki,Ninomiya, Ichiya,Date, Tadamasa,Okamura, Kimio

, p. 8119 - 8128 (2007/10/02)

A stereocontrolled synthesis of (±)-diltiazem by applying nucleophilic addition of 2-aminothiophenol to α-alkoxycinnamic acid derivatives is described.

One-Pot Preparation of α-Cyanovinyl Ethers (2-Alkoxy-2-alkenenitriles) from Vinyl Ethers: Elaboration to 3-Alkoxy-2-oxo-3-alkenenitriles and Aluminium Chloride-Catalyzed Cycloadditions to Cyclopentadiene

Hoffmann, H. M. R.,Giesel, Kunibert,Lies, Reinhard,Ismail, Zeinhom M.

, p. 548 - 551 (2007/10/02)

A variety of α-cyanovinyl ethers have been prepared by 3 different routes and elaborated to 3-alkoxy-2-oxo-3-alkenenitriles.The latter, in the presence of cyclopentadiene and aluminium chloride, give novel bridged 7-membered cycloadducts with loss of hydrogen cyanide.

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