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2-Propenoic acid, 3-[4-(methoxymethoxy)phenyl]-, methyl ester, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84184-55-4

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84184-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84184-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,1,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84184-55:
(7*8)+(6*4)+(5*1)+(4*8)+(3*4)+(2*5)+(1*5)=144
144 % 10 = 4
So 84184-55-4 is a valid CAS Registry Number.

84184-55-4Relevant academic research and scientific papers

Identification of cell-active lysine specific demethylase 1-selective inhibitors

Ueda, Rie,Suzuki, Takayoshi,Mino, Koshiki,Tsumoto, Hiroki,Nakagawa, Hidehiko,Hasegawa, Makoto,Sasaki, Ryuzo,Mizukami, Tamio,Miyata, Naoki

, p. 17536 - 17537 (2009)

(Chemical Equation Presented) Lysine specific demethylase 1 (LSD1) plays a key role in the regulation of gene expression by removing the methyl groups from methylated Lys4 of histone H3 (H3K4). Here we report the identification of the first small-molecule LSD1-selective inhibitors. These inhibitors show in vivo H3K4-methylating activity and antiproliferative activity and should be useful as lead structures for anticancer drugs and as tools for studying the biological roles of LSD1.

Efficient and versatile synthesis of 5-O-acylquinic acids with a direct esterification using a p-methoxybenzyl quinate as a key intermediate

Oyama, Kin-Ichi,Watanabe, Noriyuki,Yamada, Tomomi,Suzuki, Masako,Sekiguchi, Yukiko,Kondo, Tadao,Yoshida, Kumi

, p. 3120 - 3130 (2015/05/04)

An efficient and versatile synthesis of 5-O-acylquinic acids from commercially available (-)-quinic acid was accomplished. We designed p-methoxybenzyl quinate as a key intermediate, and two problems, the esterification of the sterically hindered 5-OH group for the concise divergent synthesis and the low yield of the final deprotection step, were solved. For the first problem, we improved Tanabe's method, TsCl/NMI-mediated esterification using free carboxylic acids, by the addition of i-Pr2NEt. For the second problem, we established a TFA- or BCl3/C6HMe5-catalyzed deprotection reaction for the final deprotection step. 5-O-Acylquinic acids were synthesized in seven steps with 45-60% overall yield.

METHODS OF TREATMENT USING ARYLCYCLOPROPYLAMINE COMPOUNDS

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Paragraph 0303-0304; 0308, (2014/12/09)

Described herein are methods of treating breast cancer using arylcyclopropylamine compounds.

METHODS OF TREATMENT USING ARYLCYCLOPROPYLAMINE COMPOUNDS

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Paragraph 0221; 0222; 0226, (2013/07/19)

Described herein are methods of treating Parkinson's disease using arylcyclopropylamine compounds.

Studies on the Chemical Constituents of Rutaceous Plants. Part 45. Novel Phenyl Propanoids: Cuspidiol, Boninenal, and Methyl Boninenalate

Ishii, Hisashi,Ishikawa, Tsutomu,Tohojoh, Toshiaki,Murakami, Keiko,Kawanable, Eri,et al.

, p. 2051 - 2058 (2007/10/02)

Cuspidiol, boninenal, and methyl boninenalate were established as having the structures 3-phenyl>propanol (1), (E)-3-phenyl>propenal (2), and (E)-3-phenyl>propenal (3) respectively.The three compounds were also independently synthesized.

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