1207-75-6

• 

• Basic information

  1. Product Name: 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione
  2. Synonyms: 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione;3-(2-hydroxyethyl)-1H,3H-quinazoline-2,4-dione;3-(2-HYDROXYETHYL)QUINAZOLINE-2,4-DIONE;3-(2-Hydroxyethyl)quinazoline-2,4(1H,3H)-dione;3-(2-hydroxyethyl)-1H-quinazoline-2,4-dione;3-(2-hydroxyethyl)-1H-quinazoline-2,4-quinone;MFCD00052597;3-(2-hydroxyethyl)-1,2,3,4-tetrahydroquinazoline-2,4-dione
  3. CAS NO:1207-75-6
  4. Molecular Formula: C₁₀H₁₀N₂O₃
  5. Molecular Weight: 206.198
  6. EINECS: 214-897-3
  7. Product Categories: N/A
  8. Mol File: 1207-75-6.mol
  9. Article Data: 8

• Chemical Properties

  1. Melting Point: 253.5-254 °C(Solv: water (7732-18-5); acetic acid (64-19-7))
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.361 g/cm³
  6. Vapor Pressure: 0-0Pa at 20-25℃
  7. Refractive Index: 1.6
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 12.67±0.20(Predicted)
  11. CAS DataBase Reference: 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione(CAS DataBase Reference)
  12. NIST Chemistry Reference: 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione(1207-75-6)
  13. EPA Substance Registry System: 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione(1207-75-6)

• 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: 1207-75-6(Hazardous Substances Data)

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• 2,4(1H,3H)-Quinazolinedione,3-(2-hydroxyethyl)-

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1207-75-6 Usage

General Description

3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione is a chemical compound with the molecular formula C10H10N2O3. It is a quinazoline derivative that contains a hydroxyethyl group. 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It may also have potential biological and pharmacological activities, although further research is needed to fully understand its properties and potential applications. Overall, 3-(2-Hydroxyethyl)-2,4-(1H,3H)-quinazoline-dione is an important compound in organic chemistry with potential value in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1207-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1207-75:
(6*1)+(5*2)+(4*0)+(3*7)+(2*7)+(1*5)=56
56 % 10 = 6
So 1207-75-6 is a valid CAS Registry Number.

InChI:InChI=1/C10H10N2O3/c13-6-5-12-9(14)7-3-1-2-4-8(7)11-10(12)15/h1-4,13H,5-6H2,(H,11,15)

1207-75-6SDS

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-(2-hydroxyethyl)-1H-quinazoline-2,4-dione

1.2 Other means of identification

Product number	-
Other names	3-(2-hydroxyethyl)quinazoline-2,4(1H,3H)-dione

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:1207-75-6 SDS

1207-75-6Upstream product

• 108890-73-9 ethyl 2-((ethoxycarbonyl)amino)benzoate 
• 141-43-5 ethanolamine 
• 91-56-5 indole-2,3-dione 
• 83846-67-7 methyl 2-((ethoxycarbonyl)amino)benzoate 
• 87-25-2 2-ethoxycarbonylaniline 
• 7143-42-2 methyl 2-((methoxycarbonyl)amino)benzoate 
• 82603-69-8 methyl 1,4-dihydro-2,4-dioxoquinazoline-3(2H)-acetate 
• 1885-29-6 anthranilic acid nitrile 
• 134-20-3 2-carbomethoxyaniline 
• 118-92-3 anthranilic acid 
• 77093-92-6 methyl 2-<3-(2-chloroethyl)ureido>benzoate 
• 77093-94-8 2-(2-chloroethylamino)-4H-<3,1>benzoxazin-4-one hydrochloride 
• 5081-87-8 3-(2-chloroethyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline 
• 52727-44-3 2,3-dihydro-5H-oxazolo<2,3-b>quinazolin-5-one 

1207-75-6Downstream Products

• 5081-87-8 3-(2-chloroethyl)-2,4-dioxo-1,2,3,4-tetrahydroquinazoline 
• 83846-83-7 ketanserin tartrate 
• 74050-98-9 ketanserine 
• 52727-44-3 2,3-dihydro-5H-oxazolo<2,3-b>quinazolin-5-one 
• 1029791-08-9 ethyl 2-[2,4-dioxo-1,2-dihydroquinazoline-3(4H)-yl]benzoate 

1207-75-6Relevant articles and documents

Synthesis, crystal structure, spectral and DFT studies of potent isatin derived metal complexes

Sumrra, Sajjad Hussain,Atif, Aftab Hussain,Zafar, Muhammad Naveed,Khalid, Muhammad,Tahir, Muhammad Nawaz,Nazar, Muhammad Faizan,Nadeem, Muhammad Arif,Braga, Ataualpa A.C.

, p. 110 - 120 (2018)

The isatin-core in compounds offers exciting perspectives in medicinal and pharmacological research. The present study reports the successful development of new isatin-core transition metal based anti-bacterial complexes via conventional refluxing method.

Ketoserin intermediate and preparation method of ketoserin

-

Paragraph 0045-0046; 0048-0050, (2021/01/15)

The invention discloses a preparation method of a ketoserin intermediate 2, 3-dihydro-5H-oxazolo[2, 3-B]quinazoline-5-ketone and a preparation method of ketoserin, and the reaction equation of the preparation method of the ketoserin intermediate 2, 3-dihydro-5H-oxazolo[2, 3-B]quinazoline-5-ketone is shown in the specification: in the reaction, sodium carbonate and acetonitrile are used, no catalyst is added, inorganic salt is removed through hot filtration after the reaction, filtrate is evaporated to dryness, acetonitrile is recycled, and an intermediate 04, namely the ketoserin intermediate2, 3-dihydro-5H-oxazolo[2, 3-B]quinazoline-5-ketone, is obtained. The method is simple and convenient to operate, lower in cost, better in product character and more beneficial to synthesis of a finalproduct.

4-Hydroxy-2-quinolones 173. 1-R-3-(2-diethylamino- ethyl)-1H-quinazoline- 2,4-dione hydrochlorides as potential local anesthetic agents

Ukrainets,Kravtsova,Tkach,Mamchur,Kovalenko, E. Yu.

experimental part, p. 96 - 105 (2010/09/04)

Different variants of the preparation and procedures in the synthesis of a series of 1-R-3-(2-dialkyl-aminoethyl)-1H-quinazoline-2,4-dione hydrochlorides having a structural similarity to the 4-hydroxy-2-quinolinone anesthetic chinoxicaine are discussed. A comparative analysis of the biological properties of the synthesized compounds and the known local anesthetics chinoxicaine and lidocaine is reported.

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