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4-Hydroxy-1-(4-nitrophenyl)piperidine is a chemical compound that belongs to the class of piperidine derivatives. It is characterized by a white to yellow solid appearance and a molecular formula of C11H14N2O3. 4-Hydroxy-1-(4-nitrophenyl)piperidine features a 4-nitrophenyl substituent attached to the piperidine ring, along with a hydroxyl group at the C-4 position. Its structural attributes and potential biological activities make it a significant compound in the fields of pharmaceuticals and agrochemicals, with applications in drug research and development.

79421-45-7

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79421-45-7 Usage

Uses

Used in Pharmaceutical Synthesis:
4-Hydroxy-1-(4-nitrophenyl)piperidine is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities. Its derivatives have been studied for their potential as antipsychotic and anti-inflammatory agents, highlighting its importance in the development of new medications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-Hydroxy-1-(4-nitrophenyl)piperidine is utilized as a precursor in the production of various agrochemicals, contributing to the development of effective pest control and crop protection solutions.
Used in Drug Research and Development:
4-Hydroxy-1-(4-nitrophenyl)piperidine is employed as a valuable compound in drug research and development due to its antimicrobial and antifungal properties. These characteristics make it a promising candidate for the creation of new antimicrobial agents to combat resistant strains and improve public health.
Used in Antimicrobial Applications:
4-Hydroxy-1-(4-nitrophenyl)piperidine is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, making it a potential component in the development of new antibiotics and antifungal medications.
Used in Anti-inflammatory Applications:
4-Hydroxy-1-(4-nitrophenyl)piperidine is also used as an anti-inflammatory agent, given its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions, contributing to the advancement of treatments for various inflammatory diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 79421-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79421-45:
(7*7)+(6*9)+(5*4)+(4*2)+(3*1)+(2*4)+(1*5)=147
147 % 10 = 7
So 79421-45-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O3/c14-11-5-7-12(8-6-11)9-1-3-10(4-2-9)13(15)16/h1-4,11,14H,5-8H2

79421-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)piperidin-4-ol

1.2 Other means of identification

Product number -
Other names nitrophenylpiperidinol

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:79421-45-7 SDS

79421-45-7Relevant articles and documents

Discovery of a Pyrimidothiazolodiazepinone as a Potent and Selective Focal Adhesion Kinase (FAK) Inhibitor

Groendyke, Brian J.,Nabet, Behnam,Mohardt, Mikaela L.,Zhang, Haisheng,Peng, Ke,Koide, Eriko,Coffey, Calvin R.,Che, Jianwei,Scott, David A.,Bass, Adam J.,Gray, Nathanael S.

supporting information, p. 30 - 38 (2021/01/11)

Focal adhesion kinase (FAK) is a tyrosine kinase with prominent roles in protein scaffolding, migration, angiogenesis, and anchorage-independent cell survival and is an attractive target for the development of cancer therapeutics. However, current FAK inhibitors display dual kinase inhibition and/or significant activity on several kinases. Although multitargeted activity is at times therapeutically advantageous, such behavior can also lead to toxicity and confound chemical-biology studies. We report a novel series of small molecules based on a tricyclic pyrimidothiazolodiazepinone core that displays both high potency and selectivity for FAK. Structure-activity relationship (SAR) studies explored modifications to the thiazole, diazepinone, and aniline "tail,"which identified lead compound BJG-03-025. BJG-03-025 displays potent biochemical FAK inhibition (IC50 = 20 nM), excellent kinome selectivity, activity in 3D-culture breast and gastric cancer models, and favorable pharmacokinetic properties in mice. BJG-03-025 is a valuable chemical probe for evaluation of FAK-dependent biology.

Indazole formamide compound as well as preparation method and application thereof

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Paragraph 0084-0087, (2021/02/16)

The invention belongs to the field of chemical medicines, and particularly relates to an indazole formamide compound as well as a preparation method and application thereof. The invention provides anindazole carboxamide compound or a pharmaceutically acce

COMPOUNDS FOR TARGETED DEGRADATION OF BRD9

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Page/Page column 471-472, (2021/09/11)

BRD9 protein degradation compounds or pharmaceutically acceptable salts thereof are provided for the treatment of disorders mediated by BRD9, including but not limited to abnormal cellular proliferation.

HETEROCYCLIC COMPOUNDS AND USES THEREOF

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Paragraph 0513-0515, (2019/04/25)

Heterocyclic compounds as Wee1 inhibitors are provided. The compounds may find use as therapeutic agents for the treatment of diseases and may find particular use in oncology.

Design, synthesis and biological evaluation of novel 7-amino-[1,2,4]triazolo[4,3-f]pteridinone, and 7-aminotetrazolo[1,5-f]pteridinone derivative as potent antitumor agents

Hou, Yunlei,Zhu, Liangyu,Li, Zhiwei,Shen, Qi,Xu, Qiaoling,Li, Wei,Liu, Yajing,Gong, Ping

, p. 690 - 709 (2019/01/04)

To develop novel therapeutic agents with anticancer activities, two series of novel 7-amino-[1,2,4]triazolo[4,3-f]pteridinone, and 7-aminotetrazolo[1,5-f]pteridinone derivatives were designed and synthesized. All compounds were tested for anti-proliferative activities against five cancer cell lines. The structure-activity relationships (SARs) studies were conducted through the variation in two regions, the moiety of A ring and the terminal aniline B on pteridinone core. 1-Methyl-1,2,4-triazole derivative L7 with 2,6-dimethylpiperazine showed the most potent antiproliferative activity against A549, PC-3, HCT116, MCF-7 and MDA-MB-231 cell lines with IC50 values of 0.16 μM, 0.30 μM, 0.51 μM, 0.30 μM, and 0.70 μM, respectively. Combined with the results of the molecular docking and enzymatic studies, the PLK1 was very likely to be one of the drug targets of compound L7. Furthermore, to clarify the anticancer mechanism of compound L7, further explorations in the bioactivity were conducted. The results showed that compound L7 obviously inhibited proliferation of A549 cell lines, induced a great decrease in mitochondrial membrane potential leading to apoptosis of cancer cells, suppressed the migration of tumor cells, and arrested G1 phase of A549 cells.

2,4-dibasic miazines compound

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Paragraph 0277; 0278; 0279; 0280, (2017/08/29)

The invention belongs to the field of medical chemistry, relates to a 2,4-dibasic miazines compound and specifically relates to a compound shown as formula (I) or a pharmaceutically acceptable salt thereof, a drug compound thereof and an application thereof in treating EGFR or/and ALK mediated diseases.

COMPOUNDS FOR TREATMENT OF INFLAMMATORY DISEASES

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Paragraph 0120; 0121; 0122; 0123, (2016/10/27)

The present invention refers to relates to compound for treating inflammatory diseases, said formula I compounds represented, such as, a pharmaceutically acceptable salts, or their, or a hydrate thereof is characterized in that the, polymerized. According to the present invention, interacting with-path 5-LOX a compound or interference, in particular 5- oh height[...]width it recovers sourly, in sacrifice, which display inhibitory effects can be provides compounds having. (by machine translation)

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

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Paragraph 0356; 0357, (2014/05/08)

Provided are pyridopyrazine compounds of formula (1), pharmaceutical compositions thereof and methods of use therefore, wherein R1, R2, R3, R4 and m are as defined in the specification.

VEGFR TYROSINE KINASE INHIBITORS

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Page/Page column 30, (2014/12/12)

Novel compounds, their prodrugs, and the pharmaceutically acceptable salts as pharmaceutical compositions containing such compounds useful in treating certain diseases modulated by the inhibition of vascular endothelial growth factors (VEGFs) receptor tyrosine kinases are provided. In particular, compounds and compositions and the methods for the prophylaxis, management and treatment of cancers through the inhibition of VEGF receptor tyrosine kinases are provided.

2, 4 -DIAMINOPYRIMIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

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Page/Page column 112, (2012/05/20)

The present invention relates to novel pyrimide derivatives of formula (I): that are useful as kinase inhibitors. More particularly, the present invention relates to novel pyrimidine compounds, methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of proliferative disorders.

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