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3-(4-Hydroxy-phenyl)-3-oxo-propionitrile, also known as 3-(4-Hydroxyphenyl)-3-oxopropanenitrile or 4'-Hydroxy-3'-cyanopropiophenone, is a chemical compound that features a nitrile group and a hydroxyphenyl group. Its unique structure endows it with potential applications in pharmaceutical and chemical research, where it may exhibit useful properties due to its structural features.

70591-87-6

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70591-87-6 Usage

Uses

Used in Pharmaceutical Research:
3-(4-HYDROXY-PHENYL)-3-OXO-PROPIONITRILE is used as a key intermediate in the synthesis of various organic compounds for pharmaceutical applications. Its structural features allow it to be a versatile building block in the development of new drugs with potential biological activity.
Used in Chemical Research:
In the field of chemical research, 3-(4-HYDROXY-PHENYL)-3-OXO-PROPIONITRILE is utilized as a reagent or starting material for the synthesis of complex organic molecules. Its nitrile and hydroxyphenyl groups can participate in various chemical reactions, contributing to the creation of novel chemical entities.
Used in Synthesis of Organic Compounds:
3-(4-HYDROXY-PHENYL)-3-OXO-PROPIONITRILE is used as a precursor in the synthesis of a wide range of organic compounds. Its ability to be modified and incorporated into larger molecules makes it a valuable component in organic chemistry for creating new materials and compounds with specific properties.
The specific properties and potential applications of 3-(4-Hydroxy-phenyl)-3-oxo-propionitrile may vary depending on its use case and the conditions under which it is employed, highlighting its adaptability across different scientific domains.

Check Digit Verification of cas no

The CAS Registry Mumber 70591-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,9 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70591-87:
(7*7)+(6*0)+(5*5)+(4*9)+(3*1)+(2*8)+(1*7)=136
136 % 10 = 6
So 70591-87-6 is a valid CAS Registry Number.

70591-87-6SDS

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 3-(4-Hydroxyphenyl)-3-oxopropanenitrile

1.2 Other means of identification

Product number -
Other names 4-(Cyanoacetyl)phenol

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:70591-87-6 SDS

70591-87-6Downstream Products

70591-87-6Relevant articles and documents

Microwave synthesis of 1-aryl-1H-pyrazole-5-amines

Everson, Nikalet,Yniguez, Kenya,Loop, Lauren,Lazaro, Horacio,Belanger, Briana,Koch, Grant,Bach, Jordan,Manjunath, Aashrita,Schioldager, Ryan,Law, Jarvis,Grabenauer, Megan,Eagon, Scott

, p. 72 - 74 (2018/11/30)

A microwave-mediated synthesis of 1H-pyrazole-5-amines utilizing 1 M HCl at 150 °C was developed in order to provide products in a matter of minutes with minimal purification. Most reactions are complete in only 10 min and can be isolated via a simple filtration without the need for further purification by column chromatography or recrystallization. This method tolerates a range of functional groups and can be performed on milligram to gram scales.

Synthesis of Phenols: Organophotoredox/Nickel Dual Catalytic Hydroxylation of Aryl Halides with Water

Yang, Liu,Huang, Zhiyan,Li, Gang,Zhang, Wei,Cao, Rui,Wang, Chao,Xiao, Jianliang,Xue, Dong

supporting information, p. 1968 - 1972 (2018/02/06)

A highly effective hydroxylation reaction of aryl halides with water under synergistic organophotoredox and nickel catalysis is reported. The OH group of the resulting phenols originates from water, following deprotonation facilitated by an intramolecular base group on the ligand. Significantly, aryl bromides as well as less reactive aryl chlorides served as effective substrates to afford phenols with a wide range of functional groups. Without the need for a strong inorganic base or an expensive noble-metal catalyst, this process can be applied to the efficient preparation of diverse phenols and enables the hydroxylation of multifunctional pharmaceutically relevant aryl halides.

Potential antiarthritic agents. II. Benzoylacetonitriles and β-aminocinnamonitriles

Ridge,Hanifin,Harten,Johnson,Menschik,Nicolau,Sloboda,Watts

, p. 1385 - 1389 (2007/10/09)

Benzoylacetonitrile and β-aminocinnamonitrile are shown to possess potent intiinflammatory activity in the rat adjuvant arthritis model. In a series of phenyl-substituted analogues, only o-, m-, and p-fluorobenzoylacetonitrile and m- and p-fluoro-β-aminocinnamonitrile retained activity. Additionally, β-amino-2- and β-amino-3-thiopheneacrylonitrile and β-oxo-2- and β-oxo-3-thiophenepropionitrile exhibited similar activity. These agents are not believed to be acting via prostaglandin synthetase inhibition. The metabolic profile of benzoylacetonitrile is also described.

BETA-ADRENERGIC BLOCKING AGENTS IN THE 1,2,3-THIADIAZOLE SERIES

-

, (2008/06/13)

Novel 4-2,3 or 4(3-amino-2-hydroxypropoxy) phenyl!-and 5-2, 3 or 4(3-amino-2-hydroxypropoxy) phenyl!-1,2,3-thiadiazole derivatives which may be further substituted at the C-5 or C-4 position of the thiadiazole ring, respectively, by a lower alkyl, phenyl, trifluoromethyl, carboxy, alkoxycarbonyl, cyano or an aminocarbonyl group, and the pharmaceutically acceptable acid addition salts thereof and processes for the production of such compounds; 4-4(3-t-butylamino-2-hydroxypropoxy) phenyl!-1,2,3-thiadiazole and 5-4(3-t-butylamino-2-hydroxypropoxy) phenyl!-1,2,3-thiadiazole are representative of the class. These compounds possess cardiovascular activity and are useful for the treatment of abnormal heart conditions in mammals.

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