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6-chloro-4-cyclopropyl-1-(4-methoxybenzyl)-quinazolin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150878-37-8

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150878-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150878-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 150878-37:
(8*1)+(7*5)+(6*0)+(5*8)+(4*7)+(3*8)+(2*3)+(1*7)=148
148 % 10 = 8
So 150878-37-8 is a valid CAS Registry Number.

150878-37-8Relevant articles and documents

Synthesis of a series of 4-(arylethynyl)-6-chloro-4-cyclopropyl-3,4- dihydroquinazolin-2(1H)-ones as novel non-nucleoside HIV-1 reverse transcriptase inhibitors

Tucker,Lyle,Wiscount,Britcher,Young,Sanders,Lumma,Goldman,O'Brien,Ball,Homnick,Schleif,Emini,Huff,Anderson

, p. 2437 - 2444 (1994)

As part of an ongoing effort to prepare novel non-nucleoside inhibitors of human immunodeficiency virus type-1 (HIV-1) reverse transcriptase (RT), a series of 4-(arylethynyl)-6-chloro-4-cyclopropyl-3,4-dihydroquinazolin- 2(1H)-ones 4aa-1 has been prepared

Chiral resolution process

-

, (2008/06/13)

A chiral resolution process is described for the purification of a substituted chiral quinazoline, by salt formation with a resolving agent, followed by crystallization.

Synthesis of a New Generation Reverse Transcriptase Inhibitor via the BCl3/GaCl3-induced Condensation of Anilines with Nitriles (Sugasawa Reaction)

Houpis, Ioannis N.,Molina, Audrey,Douglas, Alan W.,Xavier, Lyndon,Lynch, Joseph,et al.

, p. 6811 - 6814 (2007/10/02)

The synthesis of 1 was achieved in high overall yield through a mechanism-based improvement of the preparation of o-acyl anilines.

New quinazolines as inhibitors of HIV reverse transcriptase

-

, (2008/06/13)

Compounds having a quinazolin-2-one nucleus with a substituted alkynyl or substituted alkenyl at the 4-position are described. These compounds are useful in the inhibition of HIV reverse transcriptase (including its resistant varieties), the prevention or

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