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3,4-Dihydroquinazoline is a heterocyclic organic compound with the molecular formula C8H7N. It is a reduced form of quinazoline, which is a tricyclic fused-ring system consisting of a benzene ring fused to a pyrazine ring. Quinazoline, 3,4-dihydro- is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, as it can be easily functionalized and transformed into a wide range of biologically active molecules. 3,4-Dihydroquinazoline derivatives have been found to possess diverse biological activities, including anticancer, antiviral, and anti-inflammatory properties. The compound can be synthesized through various methods, such as the condensation of o-aminobenzylamines with formic acid or the reduction of quinazoline using hydrogenation techniques. Due to its potential applications in drug discovery and development, 3,4-dihydroquinazoline continues to be an area of interest for researchers in the field of medicinal chemistry.

1904-64-9

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1904-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1904-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1904-64:
(6*1)+(5*9)+(4*0)+(3*4)+(2*6)+(1*4)=79
79 % 10 = 9
So 1904-64-9 is a valid CAS Registry Number.

1904-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dihydro quinazoline

1.2 Other means of identification

Product number -
Other names 3,4-Dihydroguinazolin

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:1904-64-9 SDS

1904-64-9Relevant academic research and scientific papers

Cu@U-g-C3N4 Catalyzed Cyclization of o-Phenylenediamines for the Synthesis of Benzimidazoles by Using CO2 and Dimethylamine Borane as a Hydrogen Source

Phatake, Vishal V.,Bhanage, Bhalchandra M.

, p. 347 - 359 (2019)

Abstract: This work reports a green and sustainable route for the synthesis of benzimidazoles via C–N bond formation using carbon dioxide (CO2) as a C1 carbon source. In this work, Cu@U-g-C3N4 catalyst was prepared from urea derived porous graphitic carbon?nitride (U-g-C3N4) and CuCl2 and characterized by FT-IR, XRD, XPS, SEM, TPD etc. The Cu@U-g-C3N4 as a heterogeneous recyclable catalyst has been employed first time for the cyclization of o-phenylenediamines (OPD) with CO2 to benzimidazoles using dimethylamine borane (DMAB). The proposed protocol becomes sustainable and efficient due to the use of propylene carbonate/water as a suitable biodegradable, economical and environmentally benign solvent system. The proposed catalytic system showed a wide range of substrate scope for the synthesis of benzimidazoles in good to excellent yields. Graphical Abstract: [Figure not available: see fulltext.]

Chemoselective hydrogenation of heteroarenes and arenes by Pd-Ru-PVP under mild conditions

Abe, Naoya,Chaudhari, Chandan,Ikeda, Yasuyuki,Kitagawa, Hiroshi,Kusuda, Kohei,Matsumura, Syo,Nagaoka, Katsutoshi,Nishida, Yoshihide,Sato, Katsutoshi,Terada, Kenji,Toriyama, Takaaki,Yamamoto, Tomokazu

, p. 44191 - 44195 (2020/12/25)

Monometallic (Pd, Ru or Rh) and bimetallic (Pd0.5-Ru0.5) alloy NPs catalysts were examined for the hydrogenation of quinoline. Pd-Ru alloy catalyst showed superior catalytic activity to the traditional Rh catalyst. The characterization of Pd0.5-Ru0.5 catalysts, HAADF-EDX mapping and XPS analysis suggested that the alloy state of PdRu catalysts remained unchanged in the recovered catalyst. Furthermore, the catalyst was highly selective for the hydrogenation of different arenes. This journal is

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