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5-Hydroxyphenanthridin-6(5H)-one is a naturally occurring chemical compound belonging to the phenanthridinone class, characterized by its unique structure and properties. 5-hydroxyphenanthridin-6(5H)-one is derived from the phenanthridine alkaloid family, which is known for its diverse range of biological activities, including antitumor, antiviral, and antimicrobial effects. The presence of a hydroxyl group at the 5-position and a carbonyl group at the 6-position in its structure contributes to its reactivity and potential applications in medicinal chemistry. Research on 5-hydroxyphenanthridin-6(5H)-one and its derivatives is ongoing, as scientists explore their potential therapeutic uses and mechanisms of action.

7605-71-2

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7605-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7605-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,0 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7605-71:
(6*7)+(5*6)+(4*0)+(3*5)+(2*7)+(1*1)=102
102 % 10 = 2
So 7605-71-2 is a valid CAS Registry Number.

7605-71-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Benzoyloxymethyl-5-hydroxy-4H-pyran-4-on

1.2 Other means of identification

Product number -
Other names 2-benzoyloxymethyl-5-hydroxy-pyran-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7605-71-2 SDS

7605-71-2Downstream Products

7605-71-2Relevant academic research and scientific papers

Iron and transition metal transport into erythrocytes mediated by nifedipine degradation products and related compounds

Savigni, Donna L.,Wege, Dieter,Cliff, Garth S.,Meesters, Mark L.H.,Morgan, Evan H.

, p. 1215 - 1226 (2007/10/03)

The aim of this investigation was to determine the mechanism of action of the nitrosophenylpyridine derivative of nifedipine ("nitrosonifedipine", NN) on Fe(II) transport into erythrocytes. Nifedipine is rapidly degraded to NN by daylight. We used rabbit erythrocytes, NN, and several chemically related substances, and examined their effects on the transfer of iron and other transition metals (cadmium, cobalt, manganese, nickel, zinc) into and out of the cells. NN mediated the transfer of iron and zinc but not the other metals into the cell cytosol. The transfer of Fe(II) was not affected by changes in cell membrane potential and could not be ascribed to free radical production. Two hydroxamic acid compounds chemically related to NN also stimulated iron and zinc uptake, but no evidence was obtained for cell-induced transformation of NN to them. In vivo, NN is probably converted to a lactam derivative. This compound was found to have no effect on iron uptake by the cells. It is concluded that NN has a relatively high specificity for the transport of iron compared with other transition metals, and small changes in its structure markedly affect this action. Also, because the lactam to which NN is converted in vivo is inactive, it is unlikely that nifedipine will affect iron metabolism after therapeutic administration.

CYCLIZATION WITH NITRENIUM IONS GENERATED FROM N-METHOXY- OR N-ALLYLOXY-N-CHLOROAMIDES WITH ANHYDROUS ZINC ACETATE. SYNTHESIS OF N-HYDROXY- AND N-METHOXYNITROGEN HETEROCYCLIC COMPOUNDS

Kikugawa, Yasuo,Shimada, Masahiro,Matsumoto, Kazuhiro

, p. 293 - 302 (2007/10/02)

Electrophilic intramolecular aromatic substitution with an N-methoxy- or an N-allyloxyacylnitrenium ion, generated by treatment of an N-methoxy- or an N-allyloxy-N-chloroamide with anhydrous zinc acetate in nitromethane, leads to formation of a nitrogen h

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