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Benzenemethanol, 4-(acetyloxy)-, nitrate, also known as 4-hydroxybenzyl alcohol acetate nitrate, is a chemical compound with the molecular formula C9H11NO5. It is a derivative of benzyl alcohol, where the hydroxyl group is acetylated and the molecule is further nitrated. Benzenemethanol, 4-(acetyloxy)-, nitrate is characterized by its aromatic structure, with a benzene ring and a hydroxymethyl group attached to the para position. The acetate group provides additional functionality, while the nitrate group is a strong oxidizer. Benzenemethanol, 4-(acetyloxy)-, nitrate is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is important to handle this substance with care due to its potential reactivity and the presence of a nitrate group, which can be hazardous under certain conditions.

91735-04-5

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91735-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91735-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91735-04:
(7*9)+(6*1)+(5*7)+(4*3)+(3*5)+(2*0)+(1*4)=135
135 % 10 = 5
So 91735-04-5 is a valid CAS Registry Number.

91735-04-5Downstream Products

91735-04-5Relevant articles and documents

COMPOUNDS USEFUL IN THE TREATMENT OF NEOPLASTIC DISEASES

-

, (2015/04/15)

The present invention refers to compounds of formula: (formula A), wherein R1 is selected from (formula I), (formula II), (formula (III), (formula IV), (formula V), or (formula B), and wherein R2, R3, R4 and Rs

Chemical insights in the concept of hybrid drugs: The antitumor effect of nitric oxide-donating aspirin involves a quinone methide but not nitric oxide nor aspirin

Hulsman, Niels,Medema, Jan Paul,Bos, Carina,Jongejan, Aldo,Leurs, Rob,Smit, Martine J.,De Esch, Iwan J. P.,Richel, Dick,Wijtmans, Maikel

, p. 2424 - 2431 (2008/02/03)

Hybrid drug 1 (NO-ASA) continues to attract intense research from chemists and biologists alike. It consists of ASA and a -ONO2 group connected through a spacer and is in preclinical development as an antitumor drug. We report that, contrary to current beliefs, neither ASA nor NO contributes to this antitumor effect. Rather, an unsubstituted QM was identified as the sole cytotoxic agent. QM forms from 1 after carboxylic ester hydrolysis and, in accordance with the HSAB theory, selectively reacts with cellular GSH, which in turn triggers cell death. Remarkably, a derivative lacking ASA and the -ONO 2 group is 10 times more effective than 1. Thus, our data provide a conclusive molecular mechanism for the antitumor activity of 1. Equally importantly, we show for the first time that a "presumed invisible" linker in a hybrid drug is not so invisible after all and is in fact solely responsible for the biological effect.

PHOTOCHEMICAL NITROOXYLATION OF METHYLBENZENES BY CERIUM(IV) AMMONIUM NITRATE IN ACETONITRILE

Baciocchi, E.,Rol, C.,Sebastiani, G. V.,Serena, B.

, p. 1945 - 1946 (2007/10/02)

The photochemical reaction of substituted toluenes with CAN in CH3CN leads to good yields of benzyl nitrates under very mild conditions.

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