14484-44-7

• 

• Basic information

  1. Product Name: viridicatol
  2. Synonyms: viridicatol;3-Hydroxy-4-(3-hydroxyphenyl)-2(1H)-quinolinone;3-Hydroxy-4-(3-hydroxyphenyl)quinolin-2(1H)-one;3-Hydroxy-4-(m-hydroxyphenyl)carbostyril
  3. CAS NO:14484-44-7
  4. Molecular Formula: C₁₅H₁₁NO₃
  5. Molecular Weight: 253.25
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 14484-44-7.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 553.4°Cat760mmHg
  3. Flash Point: 288.5°C
  4. Appearance: /
  5. Density: 1.425g/cm³
  6. Vapor Pressure: 4.43E-13mmHg at 25°C
  7. Refractive Index: 1.709
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: viridicatol(CAS DataBase Reference)
  11. NIST Chemistry Reference: viridicatol(14484-44-7)
  12. EPA Substance Registry System: viridicatol(14484-44-7)

• 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: 14484-44-7(Hazardous Substances Data)

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• 3-hydroxy-4-(3-hydroxyphenyl)-1H-quinolin-2-one

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14484-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14484-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,8 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14484-44:
(7*1)+(6*4)+(5*4)+(4*8)+(3*4)+(2*4)+(1*4)=107
107 % 10 = 7
So 14484-44-7 is a valid CAS Registry Number.

InChI:InChI=1/C15H11NO3/c17-10-5-3-4-9(8-10)13-11-6-1-2-7-12(11)16-15(19)14(13)18/h1-8,17-18H,(H,16,19)

14484-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	viridicatol

1.2 Other means of identification

Product number	-
Other names	Viridicatol

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:14484-44-7 SDS

14484-44-7Upstream product

• 62-53-3 aniline 
• 3526-43-0 N-(4-methoxybenzyl)aniline 
• 836-41-9 p-methoxybenzylidene-phenylamine 
• 91-56-5 indole-2,3-dione 
• 100-83-4 meta-hydroxybenzaldehyde 
• 1134192-62-3 3-hydroxy-4-(3-hydroxyphenyl)-1-(4-methoxybenzyl)quinolin-2(1H)-one 

14484-44-7Downstream Products

14484-44-7Relevant articles and documents

Synthesis of 3-Hydroxy-4-arylquinolin-2-ones Including Viridicatol via a Darzens Condensation/Friedel-Crafts Alkylation Strategy

Mamedov, Vakhid A.,Mamedova, Vera L.,Kadyrova, Saniya F.,Galimullina, Venera R.,Khikmatova, Gul'Naz Z.,Korshin, Dmitry E.,Gubaidullin, Aidar T.,Krivolapov, Dmitry B.,Rizvanov, Il'Dar Kh.,Bazanova, Olga B.,Sinyashin, Oleg G.,Latypov, Shamil K.

, p. 13132 - 13145 (2018/10/31)

The new efficient synthesis of biologically important 3-hydroxy-4-arylquinolin-2-ones through the Darzens condensation (epoxidation) of dichloroacetanilides with aromatic aldehydes followed by one-pot dechlorative epoxide-arene cyclization is described. T

A concise and versatile synthesis of viridicatin alkaloids from cyanoacetanilides

Kobayashi, Yusuke,Harayama, Takashi

supporting information; experimental part, p. 1603 - 1606 (2009/08/07)

The efficient synthesis of 3-hydroxy-4-arylquinolin-2(1H)-ones through one-pot Knoevenagel condensation/epoxidation of cyanoacetanilides followed by decyanative epoxide-arene cyclization is described. A convergent assembly with functionalized aldehydes allows for rapid synthesis with diverse substitution patterns. Isolation of 3-hydroxy-4-arylquinolin-2(1H)-ones is readily accomplished by precipitation and filtration.

Thermal degradation and mass spectrometry of benzodiazepine alkaloids (minus)-cyclopenin and (minus)-cyclopenol

Luckner,Winter,Nover,Reisch

, p. 2575 - 2588 (2007/10/04)

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