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60708-98-7

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60708-98-7 Usage

Class

Quinazoline

Type

Polycyclic aromatic hydrocarbon

Pharmacological properties

a. Antioxidant activity
b. Anti-inflammatory activity
c. Anti-tumor activity

Investigated for

a. Impact on neurological diseases and conditions
b. Potential therapy for certain types of cancer

Research and development potential

Medicine and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 60708-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,0 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60708-98:
(7*6)+(6*0)+(5*7)+(4*0)+(3*8)+(2*9)+(1*8)=127
127 % 10 = 7
So 60708-98-7 is a valid CAS Registry Number.

60708-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenyl-1,2-dihydro-benzo[f]quinazoline

1.2 Other means of identification

Product number -
Other names 1,3-Diphenyl-1,2-dihydro-benzo[f]quinazoline

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:60708-98-7 SDS

60708-98-7Downstream Products

60708-98-7Relevant articles and documents

Catalyst- and solvent-free, pot, atom and step economic synthesis of tetrahydroquinazolines by an aza-Diels-Alder reaction strategy

Bhuyan, Debajyoti,Sarma, Rupam,Dommaraju, Yuvaraj,Prajapati, Dipak

supporting information, p. 1158 - 1162 (2014/03/21)

A pot, atom and step economic (PASE) synthesis of tetrahydroquinazolines has been achieved via a microwave-assisted four-component catalyst- and solvent-free aza-Diels-Alder reaction strategy. The key step of the methodology is the in situ generation of both the diene and the dienophile and their subsequent reaction to give the desired product.

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