Welcome to LookChem.com Sign In|Join Free
  • or
6-Chloro-4-phenylquinazolin-2-carboxaldehyde is an organic compound with the molecular formula C16H10ClNO2. It is a derivative of quinazolin-2-carboxaldehyde, featuring a chlorine atom at the 6th position and a phenyl group at the 4th position. 6-Chloro-4-phenylquinazolin-2-carboxaldehyde is known for its potential applications in various fields due to its unique chemical structure and properties.

5958-05-4

Post Buying Request

5958-05-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5958-05-4 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-4-phenylquinazolin-2-carboxaldehyde is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific receptors or enzymes in the body.
Used in Chemical Research:
In the field of chemical research, 6-Chloro-4-phenylquinazolin-2-carboxaldehyde serves as a valuable compound for studying the properties and reactivity of quinazolinone derivatives. It can be used to explore new reaction pathways and develop novel synthetic methods for related compounds.
Used in Material Science:
6-Chloro-4-phenylquinazolin-2-carboxaldehyde may also find applications in material science, particularly in the development of new materials with specific properties. Its unique structure could potentially be utilized in the creation of advanced materials for various applications, such as sensors, catalysts, or optoelectronic devices.

Check Digit Verification of cas no

The CAS Registry Mumber 5958-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5958-05:
(6*5)+(5*9)+(4*5)+(3*8)+(2*0)+(1*5)=124
124 % 10 = 4
So 5958-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H16O4/c1-21-16-9-8-14(17(12-16)22-2)10-15-11-18(23-19(15)20)13-6-4-3-5-7-13/h3-12H,1-2H3/b15-10-

5958-05-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • USP

  • (1483039)  Oxazepam Related Compound C  United States Pharmacopeia (USP) Reference Standard

  • 5958-05-4

  • 1483039-15MG

  • 14,500.98CNY

  • Detail

5958-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-4-phenylquinazoline-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-chloro 4-phenyl quinazoline 2 carboxaldehyde

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:5958-05-4 SDS

5958-05-4Relevant academic research and scientific papers

Preparation process of oxazepam impurity II

-

Paragraph 0029-0059, (2020/10/30)

The invention provides a preparation process of an oxazepam impurity II, which comprises the following steps: by using oxazepam as a raw material, adding a catalyst pyruvic acid into a dipole solvent,carrying out heat preservation reaction, and carrying o

Facile thermal rearrangement of Lorazepam and Oxazepam

Siddegowda, Maravanahalli S.,Yathirajan, Hemmige S.,Ramakrishn, Ramesha A.

, p. 1628 - 1632 (2013/01/15)

Lorazepam 1, a very well known anti-convulsant undergo facile thermal rearrangement at about 110°C to 6-chloro-4-(ochlorophenyl)-2- Quinazolinecarboxaldehyde 10 in almost quantitative yield. Oxazepam 2 which is structurally similar, require higher tempera

Characterization of lorazepam and oxazepam by the thermal behavior of their degradation product

Chauvet

, p. 256 - 260 (2007/10/02)

Lorazepam and oxazepam are benzodiazepine which differ by the presence, or not, of chlorine atom on the phenyl ring. These molecules are able of chemical and thermal degradation with water intramolecular elimination between hydroxy and amine functional gr

Characterization of the Fluorescence Derivatization Products of Oxazepam in Mixtures of Acetic Acid and Methanol

Escobal, Ana R.,Iriondo, Carmen,Berrueta, Luis A.,Gallo, Blanca,Vicente, Francisca

, p. 1937 - 1947 (2007/10/02)

The fluorescence of oxazepam in mixtures of acetic acid and methanol was studied.The two reaction products were isolated by semi-preparative High Performance Liquid Chromatography, characterized by pmr, cmr, ir, and ms and identified as 6-chloro-4-phenylq

Quantitative -Elimination of Water from Oxazepam

Kaupp, Gerd,Knichala, Bernd

, p. 462 - 467 (2007/10/02)

Upon heating to 150 deg C, the 1,4-benzodiazepine derivative 1 (oxazepam) eliminates water to form the quinazolinecarbaldehyde 2 quantitatively.This reaction is termed a -elimination and is discussed mechanistically.Deuterium labelling experiment

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5958-05-4