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Benzeneacetic acid, 2-nitro-4-(phenylmethoxy)-, also known as 2-nitro-4-(phenylmethoxy)benzeneacetic acid, is an organic compound with the chemical formula C14H11NO5. It is a derivative of benzeneacetic acid, featuring a nitro group at the 2-position and a phenylmethoxy group at the 4-position. Benzeneacetic acid, 2-nitro-4-(phenylmethoxy)- is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structural features.

6860-79-3

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6860-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6860-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,6 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6860-79:
(6*6)+(5*8)+(4*6)+(3*0)+(2*7)+(1*9)=123
123 % 10 = 3
So 6860-79-3 is a valid CAS Registry Number.

6860-79-3Relevant academic research and scientific papers

Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, pyrazolopyridines, isothiazolopyridines, and preparation and uses thereof

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Page/Page column 68, (2010/11/26)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nACh receptors), activation of nACh receptors, and the treatment of disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (e.g., indazoles and benzothiazoles), which act as ligands for the α7 nACh receptor subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

1 H-INDAZOLES, BENZOTHIAZOLES, 1,2-BENZOISOXAZOLES, 1,2-BENZOISOTHIAZOLES, AND CHROMONES AND PREPARATION AND USES THEREOF

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Page/Page column 78, (2010/11/27)

The present invention relates generally to the field of ligands for nicotinic acetylcholine receptors (nAChR), activation of nAChRs, and the treatment of -disease conditions associated with defective or malfunctioning nicotinic acetylcholine receptors, especially of the brain. Further, this invention relates to novel compounds (indazoles and benzothiazoles), which act as ligands for the α7 nAChR subtype, methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

A novel class of achiral seco-analogs of CC-1065 and the duocarmycins: Design, synthesis, DNA binding, and anticancer properties

Kupchinsky, Stanley,Centioni, Sara,Howard, Tiffany,Trzupek, John,Roller, Shane,Carnahan, Virginia,Townes, Heather,Purnell, Bethany,Price, Carly,Handl, Heather,Summerville, Kaitlin,Johnson, Kimberly,Toth, James,Hudson, Stephen,Kiakos, Konstantinos,Hartley, John A.,Lee, Moses

, p. 6221 - 6236 (2007/10/03)

The synthesis, DNA binding properties, and in vitro and in vivo anticancer activity of fifteen achiral seco-cyclopropylindoline (or achiral seco-CI) analogs (5a-o) of CC-1065 and the duocarmycins are described. The achiral seco-CI analogs contain a 4-hydr

Compositions and methods of the use thereof achiral analogues of CC-1065 and the duocarmycins

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Page column 27, (2010/02/05)

The present invention relates to novel achiral seco-analogues of DNA minor groove and sequence-selective alkylating agents (+)-CC1065 and the duocarmycins, depicted as general class I, II, III, IV and V: wherein X is a good leaving group, such as a chlori

Compositions and methods of the use thereof achiral analogues of CC-1065 and the duocarmycins

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, (2008/06/13)

The present invention relates to novel achiral seco-analogues of the DNA minor groove and sequence-selective alkylating agents (+)-CC1065 and the duocarmycins, depicted as general class I, II III, IV and V: wherein X is a good leaving group, such as a chl

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