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38791-62-7

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38791-62-7 Usage

Description

4-Phenoxyphthalonitrile, a C4-substituted phthalonitrile, is a chemical compound known for its monoamine oxidase inhibitory activity. This property makes it a valuable component in various applications, particularly in the fields of organic pigments, dyes, and pharmaceuticals.

Uses

Used in Organic Pigments and Dyes Industry:
4-Phenoxyphthalonitrile is used as a key component in the production of organic pigments and dyes. Its unique chemical structure contributes to the development of vibrant and stable colorants that are widely utilized in various industries, such as textiles, plastics, and printing.
Used in Pharmaceutical Applications:
4-Phenoxyphthalonitrile is used as a monoamine oxidase inhibitor in the pharmaceutical industry. Monoamine oxidase inhibitors are a class of drugs that help regulate the levels of certain neurotransmitters in the brain, such as serotonin, norepinephrine, and dopamine. By inhibiting the activity of monoamine oxidase enzymes, 4-Phenoxyphthalonitrile can potentially be used in the treatment of various psychiatric and neurological disorders, including depression, anxiety, and Parkinson's disease.
Used in Dyes and Metabolites Research:
4-Phenoxyphthalonitrile's monoamine oxidase inhibitory activity also makes it a valuable compound for research in the field of dyes and metabolites. Its ability to modulate neurotransmitter levels can provide insights into the development of new drugs and therapies for various medical conditions. Additionally, its chemical properties may be useful in the synthesis of novel dyes and metabolites with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 38791-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,9 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38791-62:
(7*3)+(6*8)+(5*7)+(4*9)+(3*1)+(2*6)+(1*2)=157
157 % 10 = 7
So 38791-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H8N2O/c15-9-11-6-7-14(8-12(11)10-16)17-13-4-2-1-3-5-13/h1-8H

38791-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Phenoxyphthalonitrile

1.2 Other means of identification

Product number -
Other names 4-PHENOXY-PHTHALONITRILE

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:38791-62-7 SDS

38791-62-7Relevant articles and documents

Titanyl phthalocyanine and its soluble derivatives: Highly efficient photosensitizers for singlet oxygen production

Zhang, Xian-Fu,Wang, Yun,Niu, Lihong

, p. 232 - 237 (2010)

The photophysical properties of titanyl phthalocyanine (TiOPc), tetra(β-phenoxy) titanyl phthalocyanine (TiOPc(β-OPh)4) and tetra(α-phenoxy) titanyl phthalocyanine (TiOPc(α-OPh)4), were investigated in homogeneous solution. Absorptio

Synthesis and structural characterization of Cr(III) complex of porphyrazine and phthalocyanine derivatives: Kinetic studies of metalation and redox activity

Isabirye, David A.,Seheri, Naledi H.,Aiyelabola, Temitayo O.

, p. 489 - 495 (2017/02/19)

Chromium(III) complexes of 2,3,7,8,12,13,17,18-octakis(propyl)porphyrazine and 2,3,9,10,16,17,23,24-octa substituted phthalocyanine were synthesized, characterized and the kinetics of metalation and redox activity studied and reported. The results obtained indicated that the rate of incorporation of Cr(III) into the central cavity of the ligands is a function of the kinetic inertness and size of the metal ion as well as the peripheral substituents of the ligand. The Cr(III) complex of 2,3,7,8,12,13,17,18-octakis(propyl)porphyrazine exhibited a metal based reduction. Hence it was concluded that the nature of the incorporated metal ions has an influence on the rate and mechanism of incorporation of the metal ion and also the redox activities of these complexes.

CRYSTAL TYPES OF COMPOUNDS INHIBITING ACTIVITY OF PROLYL HYDROXYLASE AND USE THEREOF

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Paragraph 0145; 0147; 0148, (2017/10/27)

The invention relates to crystal types of compound shown as structural formula I, methods of preparing the compound, intermediate, pharmaceutical composition, and use of treating disease or pharmaceutical preparations for treating disease.

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