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160522-88-3

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160522-88-3 Usage

General Description

2,4-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]pyrimidine is a chemical compound with a complex molecular structure. It is composed of a pyrimidine core with two phenyl groups, each containing a 4,5-dihydro-1H-imidazol-2-yl substituent. 2,4-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]pyrimidine belongs to the class of pyrimidine derivatives and may have potential pharmaceutical or biochemical applications. The specific properties and uses of this chemical compound are yet to be fully elucidated, but its structural complexity and substitution pattern suggest potential for further study and development.

Check Digit Verification of cas no

The CAS Registry Mumber 160522-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,2 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 160522-88:
(8*1)+(7*6)+(6*0)+(5*5)+(4*2)+(3*2)+(2*8)+(1*8)=113
113 % 10 = 3
So 160522-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H20N6/c1-3-16(20-24-11-12-25-20)4-2-15(1)19-9-10-23-22(28-19)18-7-5-17(6-8-18)21-26-13-14-27-21/h1-10H,11-14H2,(H,24,25)(H,26,27)

160522-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]pyrimidine

1.2 Other means of identification

Product number -
Other names -

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:160522-88-3 SDS

160522-88-3Downstream Products

160522-88-3Relevant articles and documents

Anti-Pneumocystis carinii pneumonia activity of dicationic 2,4-diarylpyrimidines

Kumar,Boykin,Wilson,Jones,Bender,Dykstra,Hall,Tidwell

, p. 767 - 773 (2007/10/03)

A synthesis of 2,4-bis-(4-amidinophenyl)pyrimidine 6, 2,4-bis-[(4-imidazolin-2-yl)phenyl)]pyrimidine 7, 2,4-bis[(4-tetrahydropyrimidinyl-2-yl)phenyl]pyrimidine 8, 2,4-bis[(4-N-n-propylamidino)phenyl]pyrimidine 9, 2,4-bis[(4-N-isopropylamidino)phenyl]pyrimidine 10 and 2,4-bis[(4-N-isobutylamidino)phenyl]pyrimidine 11 starting from 4-bromobenzamidine and 4-bromoacetophenone is reported. A synthesis of 2-(4-amidinophenyl)-4-(2-methoxy-4-amidinophenyl)pyrimidine 20, 2-[4-(imidazolin-2-yl)- phenyl]-4-[2-methoxy-4-(imidazolin-2-yl)phenyl]pyrimidine 21, and 2-[4-(N-iso-propylamidino)phenyl]-4-[2-methoxy-4-(N -isopropylamidino)phenyl]pyrimidine 22 beginning with 4-bromobenzamidine and 2-methoxy-4-bromoacetophenone is described. Compounds 6-11 and 20-22 all bind strongly to DNA. Compounds 6, 9-11, and 20 given at 5 mg/kg are more active and less toxic than pentamidine at its effective dose when evaluated against Pneumocystis carinii pneumonia (PCP) in the immunosuppressed rat model. Several compounds in this series are being evaluated further as potential new anti-PCP agents.

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