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Imidazo[1,2-c]quinazolin-5(3H)-one,2,6-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38767-52-1

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38767-52-1 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 26, p. 595, 1989 DOI: 10.1002/jhet.5570260314

Check Digit Verification of cas no

The CAS Registry Mumber 38767-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,6 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38767-52:
(7*3)+(6*8)+(5*7)+(4*6)+(3*7)+(2*5)+(1*2)=161
161 % 10 = 1
So 38767-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3O/c14-10-12-8-4-2-1-3-7(8)9-11-5-6-13(9)10/h1-4H,5-6H2,(H,12,14)

38767-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dihydro-2H-imidazo[1,2-c]quinazolin-5-one

1.2 Other means of identification

Product number -
Other names 2,6-dihydro-3H-imidazo[1,2-c]quinazolin-5-one

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:38767-52-1 SDS

38767-52-1Upstream product

38767-52-1Downstream Products

38767-52-1Relevant academic research and scientific papers

Reactions of 2-aminothiobenzamide with isocyanates: A new synthesis of 2,3-dihydroimidazo[1,2-c]quinazolin-5(6H)-one and 3,4-dihydro-2H-pyrimido[1,2-c]quinazolin-6(7H)-one

Shiau,Chern,Tien,Liu

, p. 595 - 596 (2007/10/02)

2-(2-Chloroethylureido)- and 2-(3-chloropropylureido)thiobenzamides 5a,b were prepared in good yields by treating 2-aminothiobenzamide with 2-chloroethyl and 3-chloropropyl isocyanates respectively. Subsequent treatment of compound 5a and 5b either with alkali or mineral acid led to the formation of 2,3-dihydro-imidazo[1,2-c]quinazolin-5(6H)-one 7a and 3,4-dihydro-2H-pyrimido[1,2-c]quinazolin-6(7H)-one 7b.

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