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4-phenylquinazolin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14005-50-6

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14005-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14005-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,0 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14005-50:
(7*1)+(6*4)+(5*0)+(4*0)+(3*5)+(2*5)+(1*0)=56
56 % 10 = 6
So 14005-50-6 is a valid CAS Registry Number.

14005-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenylquinazolin-2-amine

1.2 Other means of identification

Product number -
Other names 4-phenyl-quinazolin-2-ylamine

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:14005-50-6 SDS

14005-50-6Relevant academic research and scientific papers

A simple and efficient approach for the synthesis of 2-aminated quinazoline derivatives via metal free oxidative annulation

Pandya, Amit N.,Villa, Eric M.,North, E. Jeffrey

, p. 1276 - 1279 (2017)

A simple and efficient approach for the synthesis of 2-aminoquinazoline derivatives in moderate to good yields. This reaction employs mild reaction conditions, is metal-free and utilizes readily available starting materials making it a more viable reaction for scale up synthesis and ligand diversity. Notably, this methodology allows for the synthesis of 2-aminoquinazolines using a free amine or cyclic amine enabling structural diversity and good atom economy.

Efficient copper-catalyzed synthesis of 2-amino-4(3h)-quinazolinone and 2-aminoquinazoline derivatives

Huang, Xuhu,Yang, Haijun,Fu, Hua,Qiao, Renzhong,Zhao, Yufen

experimental part, p. 2679 - 2688 (2010/01/21)

We have developed a versatile and efficient method for copper-catalyzed synthesis of both 2-amino-4(3H)-quinazolinone and 2-aminoquinazoline derivatives. The protocol uses readily available substituted 2-halobenzoic acids, 2-bromobenzaldehyde, 2-bromophen

Synthesis of 2-Aminoquinazolines from ortho-Fluoroketones

Hynes, John B.,Campbell, Johnny P.,Hynes, John D.

, p. 1185 - 1188 (2007/10/02)

The reactions of ten ortho-fluoroketones with guanidine carbonate in N,N-dimethylacetamide were investigated as a new synthetic approach to 2-amino-4-alkyl- and 2-amino-4-arylquinazolines.The yields obtained ranged from low to moderate and were highly dep

SYNTHESIS OF 5H-DIPYRIDOPYRIMIDIN-5-ONE AND 5-H-PYRIDOPYRIMIDOQUINAZOLIN-5-ONES

Kamal, Ahmed,Rao, Maddamsetty Venkateswara,Sattur, Pralhad Balvantrao

, p. 3075 - 3078 (2007/10/02)

α-Amino-N-heteroarenes on cyclocondensation with 2-chloropyridine-3-carboxylic acid chloride afford the title compounds 4 and 7.Although compound 4 is obtained in one-pot while compound 7 is formed via its amide intermediate 6.

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