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Pyrrolo[1,2-a]quinazoline-1,5-dione, 2,3,3a,4-tetrahydro-4-methyl-3a-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62329-95-7

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62329-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62329-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,2 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62329-95:
(7*6)+(6*2)+(5*3)+(4*2)+(3*9)+(2*9)+(1*5)=127
127 % 10 = 7
So 62329-95-7 is a valid CAS Registry Number.

62329-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-3a-phenyl-2,3,3a,4-tetrahydro-pyrrolo[1,2-a]quinazoline-1,5-dione

1.2 Other means of identification

Product number -
Other names 4-Methyl-3a-phenyl-2,3,3a,4-tetrahydro-pyrrolo[1,2-a]quinazoline-1,5-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:62329-95-7 SDS

62329-95-7Downstream Products

62329-95-7Relevant academic research and scientific papers

Efficient and convenient synthesis of pyrrolo[1,2- a ]quinazoline derivatives with the aid of tin(II) chloride

Wang, Manman,Dou, Guolan,Shi, Daqing

experimental part, p. 582 - 586 (2010/09/04)

An efficient, convenient, one-pot synthesis of 2,3,3a,4- tetrahydropyrrolo[1,2-a]quinazolin-5(1H)-one and 2,3,3a,4-tetrahydropyrrolo[1,2- a]quinazoline-1,5-dione was accomplished in good yields via the novel reductive cyclization of 2-nitrobenzamides with haloketones or keto acids mediated by SnCl22H2O system. A variety of substrates can participate in the process with good yields, making this methodology suitable for library synthesis in drug discovery efforts.

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