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5-HYDROXYVALERAMIDE, also known as 5-hydroxyhexanamide, is a chemical compound with the molecular formula C5H11NO2. It is a derivative of valeric acid and is classified as an amide. This versatile chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals, and serves as a building block in the production of various organic compounds. Notably, 5-HYDROXYVALERAMIDE is recognized for its sedative and anxiolytic properties, which suggest its potential utility in the treatment of anxiety disorders and sleep disturbances. However, further research and clinical studies are required to fully elucidate its pharmacological properties and explore its broader applications in medicine.

29686-12-2

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29686-12-2 Usage

Uses

Used in Pharmaceutical Industry:
5-HYDROXYVALERAMIDE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new medications with sedative and anxiolytic effects. Its role in this industry is crucial for creating compounds that can address anxiety disorders and sleep disturbances, pending further research and clinical validation.
Used in Agrochemical Industry:
5-HYDROXYVALERAMIDE is utilized as a component in the production of agrochemicals, where it plays a significant role in the synthesis of compounds designed to manage agricultural challenges, such as pest control and crop protection. Its amide structure allows for the creation of molecules with specific activities that can be tailored to various applications in this field.
Used in Organic Compounds Production:
As a building block, 5-HYDROXYVALERAMIDE is used in the production of a wide range of organic compounds. Its unique chemical structure makes it a valuable precursor for synthesizing complex organic molecules that can be applied across different industries, from pharmaceuticals to materials science.
While the specific applications of 5-HYDROXYVALERAMIDE in various industries are still being explored, its known properties and uses highlight its potential as a versatile compound in chemical and medicinal research. Future studies will likely uncover additional applications, expanding its utility and significance in multiple sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 29686-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,8 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29686-12:
(7*2)+(6*9)+(5*6)+(4*8)+(3*6)+(2*1)+(1*2)=152
152 % 10 = 2
So 29686-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c6-5(8)3-1-2-4-7/h7H,1-4H2,(H2,6,8)

29686-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxypentanamide

1.2 Other means of identification

Product number -
Other names 4-hydroxybutylformamide

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:29686-12-2 SDS

29686-12-2Relevant academic research and scientific papers

A mild and facile synthesis of cyclic imides using pyridinium chlorochromate

Yang, Yanyan,Wang, Ge,Cao, Xiaohui,Yan, Xilong,Chen, Ligong

, p. 657 - 658,2 (2020/07/30)

A mild and facile synthetic method of cyclic imides is presented. These compounds are widely used in the synthesis of novel medical, polymeric, photonic and electronic materials. Compared with traditional syntheses, the method reported has several advantages including mild conditions, simplified work-up and low cost.

Synthesis of 2,5-thiazole butanoic acids as potent and selective αvβ3 integrin receptor antagonists with improved oral pharmacokinetic properties

Wendt, John A.,Wu, Hongwei,Stenmark, Heather G.,Boys, Mark L.,Downs, Victoria L.,Penning, Thomas D.,Chen, Barbara B.,Wang, Yaping,Duffin, Tiffany,Finn, Mary Beth,Keene, Jeffery L.,Engleman, V. Wayne,Freeman, Sandra K.,Hanneke, Melanie L.,Shannon, Kristen E.,Nickols, Maureen A.,Steininger, Christina N.,Westlin, Marissa,Klover, Jon A.,Westlin, William,Nickols, G. Allen,Russell, Mark A.

, p. 845 - 849 (2007/10/03)

We describe a series of 2,5 thiazole containing compounds, which are potent antagonists of the integrin αvβ3 and show selectivity relative to the other integrins, such as αIIbβ 3 and αvβ6. These analogs were demonstrated to have high bioavailability relative to other relative heterocyclic analogs.

THIAZOLE COMPOUNDS AS INTEGRIN RECEPTOR ANTAGONISTS DERIVATIVES

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Page 72, (2008/06/13)

The present invention relates to pharmaceutical compositions comprising compounds of the Formula (I), and methods of selectively inhibiting or antagonizing the ανβ3 and/or the ανβ5 integrin without significantly inhibiting the ανβ6 integrin.

A mild hydration of nitriles into amides

Breuilles,Leclerc,Uguen

, p. 1401 - 1404 (2007/10/02)

Stirring mixtures of β-hydroxynitriles with manganese dioxide, deposited onto silica gel for a few days at room temperature resulted in the formation of the corresponding amides in fair to good yields. The unprecedented conversion of 3-hydroxyglutarodinitrile into the corresponding monoamide has been performed by this methodology.

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