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3-Benzyloxy-2-nitrophenyl-acetic acid is an organic compound with the molecular formula C15H13NO5. It is a derivative of phenylacetic acid, featuring a nitro group at the 2-position, a benzyloxy group at the 3-position, and a carboxylic acid group at the terminal end. 3-benzyloxy-2-nitrophenyl-acetic acid is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structural features. The presence of the nitro group can be reduced to an amine group under certain conditions, which is a common transformation in the preparation of various drugs and intermediates. The benzyloxy group provides a protecting function for the hydroxyl group, which can be removed later in the synthesis process to reveal the free hydroxyl group. 3-benzyloxy-2-nitrophenyl-acetic acid's reactivity and functional group manipulation make it a valuable building block in organic chemistry and medicinal chemistry.

6855-54-5

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6855-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6855-54-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6855-54:
(6*6)+(5*8)+(4*5)+(3*5)+(2*5)+(1*4)=125
125 % 10 = 5
So 6855-54-5 is a valid CAS Registry Number.

6855-54-5Relevant academic research and scientific papers

Antioxidative activities of oxindole-3-acetic acid derivatives from supersweet corn powder

Midoh, Naoki,Tanaka, Akihito,Nagayasu, Makiko,Furuta, Chie,Suzuki, Katsuya,Ichikawa, Takeshi,Isomura, Takashi,Nomura, Kenzo

, p. 1794 - 1801 (2011/06/17)

The components contributing to the antioxidative activity of supersweet corn powder (SSCP), which is commonly used in corn soup and snacks in Japan, were clarified and the effects investigated. 7-(0-/3-Glucosy-loxy)oxindole-3- acetic acid (GOA) was found

Synthesis of tetrahydropyrroloiminoquinone alkaloids based on electrochemically generated hypervalent iodine oxidative cyclization

Inoue, Keisuke,Ishikawa, Yuichi,Nishiyama, Shigeru

supporting information; experimental part, p. 436 - 439 (2010/04/24)

[Chemical equation presented] An approach to the synthesis of the tetrahydropyrroloiminoquinone alkaloids has been developed and applied to the preparation of N-1-βD-ribofuranosyltetrahydropyrroloiminoquinones. The strategy utilizes oxidative cyclization

5-HT4 receptor agonists

-

, (2008/06/13)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are selective agonists for 5-HT4 receptors. STR1 wherein Ak is a C3 -C6 alkyl group, and R is a C2 -C6 alkyl group, a C3 -C6 alkenyl group, a C3 -C6 alkynyl group, a C3 -C7 cycloalkyl group or a C3 -C6 cycloalkylmethyl group.

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