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67720-42-7

2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 67720-42-7 Structure

  • Basic information

    1. Product Name: 2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine
    2. Synonyms: 6-AMINO-1,2-DIHYDRO-2-OXO-4-PHENYLPYRIDINE-3,5-DICARBONITRILE;2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine
    3. CAS NO:67720-42-7
    4. Molecular Formula: C13H8N4O
    5. Molecular Weight: 236.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 67720-42-7.mol

  • Chemical Properties

    1. Melting Point: >300 °C(Solv: ethanol (64-17-5); N,N-dimethylformamide (68-12-2))
    2. Boiling Point: 414.6±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.40±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.50±0.10(Predicted)
    10. CAS DataBase Reference: 2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine(67720-42-7)
    12. EPA Substance Registry System: 2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine(67720-42-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 67720-42-7(Hazardous Substances Data)

67720-42-7 Usage

Chemical compound

2-Amino-3,5-dicyano-6-hydroxy-4-phenylpyridine

Molecular weight

248.23 g/mol

Type

Heterocyclic organic compound

Family

Pyridine family

Functional groups

Amino group (NH2), cyano group (CN), hydroxyl group (OH), and phenyl group

Biological activities

Anticancer, antiparasitic, antiviral

Potential use

Developing new drugs for various diseases

Research target

Medicinal and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 67720-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,7,2 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67720-42:
(7*6)+(6*7)+(5*7)+(4*2)+(3*0)+(2*4)+(1*2)=137
137 % 10 = 7
So 67720-42-7 is a valid CAS Registry Number.

67720-42-7SDS

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 2-amino-6-oxo-4-phenyl-1H-pyridine-3,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 6-amino-1,2-dihydro-2-oxo-4-phenylpyridine-3,5-dicarbonitrile

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:67720-42-7 SDS

67720-42-7Relevant articles and documents

Synthesis of pyrido[1,2-a][1,3,5]triazine derivatives by aminomethylation of 6-amino-4-aryl-2-oxo-1,2-dihydropyridine-3,5-dicarbonitriles

Khrustaleva,Frolov,Dotsenko,Dmitrienko,Bushmarinov,Krivokolysko

, p. 46 - 52 (2014/05/06)

The aminomethylation of 6-amino-4-aryl-2-oxo-1,2-dihydropyridine-3,5- dicarbonitriles by treatment with primary amines and an excess of formaldehyde resulted in the formation of 3-R-8-aryl-6-oxo-1,3,4,6-tetrahydro-2H-pyrido[1,2- a][1,3,5]triazine-7,9-dica

Microwave irradiation-assisted amination of 2-chloropyridine derivatives with amide solvents

Samadi, Abdelouahid,Silva, Daniel,Chioua, Mourad,Carreiras, Maria Do Carmo,Marco-Contelles, Jose

experimental part, p. 2859 - 2869 (2011/09/12)

A simple, quick, and high-yielding microwave-assisted synthesis of 2-(N,Ndimethyl) amine- and 2-aminopyridine derivatives is reported here for the first time in the reaction of 2-chloro substituted pyridines with amide solvents such as dimethylformamide or formamide, without transition-metal catalysts. Taylor & Francis Group, LLC.

An efficient and greener approach to the synthesis of 3,5-dicyanopyridin- 2(1H)-one derivatives in aqueous media under microwave irradiation conditions

Jia, Runhong,Tu, Shujiang,Zhang, Yan,Jiang, Bo,Zhang, Junyong,Yao, Changsheng,Shi, Feng

, p. 1177 - 1180 (2008/04/12)

(Chemical Equation Presented) A facile and greener synthesis of a series of 3,5-dicyanopyridin-2(1H)-one derivatives was accomplished via the one-pot reaction of aldehyde, malononitrile and sodium hydroxide in aqueous media under microwave irradiation. Th

Heterocyclic synthesis with nitriles: Synthesis of some novel pyrrolo [2,1-b]thiadiazoline, pyrrolo[2,1-b]thiadiazolo[3,2-a]pyrimidine and pyridine derivatives

Metwally, Nadia H.,Abdelrazek, Fathy M.

experimental part, p. 676 - 678 (2011/10/09)

α-(Bromothiocyanatomethyl)benzylidenemalononitrile (1) reacts with the hydrazides 2a-c, cyanoacetohydrazide (2d), cyanoacetamide (3a) and cyanoacetanilides 3b-d to afford pyrrolo[2,1-b]thiadiazolines 5a-c, pyrrolo[2,1-6]thia-diazolo[3,2-a]pyrimidine (8) and the pyridone derivatives 11a-d. Structures and conceivable mechanisms are discussed.

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