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149486-74-8

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149486-74-8 Usage

General Description

1-(2-phenylethyl)-3-(4-propyl-1,3-thiazol-2-yl)thiourea is a chemical compound with the molecular formula C16H22N2OS2. It is a thiourea derivative with a thiazole ring and a phenylethyl group. 1-(2-phenylethyl)-3-(4-propyl-1,3-thiazol-2-yl)thiourea has potential applications in the pharmaceutical and agricultural industries due to its diverse biological activities, including as an antifungal and antibacterial agent. Its unique structure and properties make it a promising candidate for further research and development in the field of medicinal chemistry and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 149486-74-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,4,8 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149486-74:
(8*1)+(7*4)+(6*9)+(5*4)+(4*8)+(3*6)+(2*7)+(1*4)=178
178 % 10 = 8
So 149486-74-8 is a valid CAS Registry Number.

149486-74-8SDS

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 1-(2-phenylethyl)-3-(4-propyl-1,3-thiazol-2-yl)thiourea

1.2 Other means of identification

Product number -
Other names PETT Analog 39

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:149486-74-8 SDS

149486-74-8Downstream Products

149486-74-8Relevant articles and documents

Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs

Bell,Cantrell,Hogberg,Jaskunas,Johansson,Jordan,Kinnick,Lind,Morin Jr.,Noreen,Oberg,Palkowitz,Parrish,Pranc,Sahlberg,Ternansky,Vasileff,Vrang,West,et al.

, p. 4929 - 4936 (2007/10/03)

A novel series of potent specific HIV-1 inhibitory compounds is described. The lead compound in the series, N-(2-phenethyl)-N'-(2-thiazolyl)thiourea (1), inhibits HIV-1 RT using rCdG as the template with an IC50 of 0.9 μM. In MT-4 cells, compound 1 inhibits HIV-1 with an ED50 of 1.3 μM. The 50% cytotoxic dose in cell culture is >380 μM. The chemical structure-activity relationship (SAR) was developed by notionally dividing the lead compound in four quadrants. The SAR strategy had two phases. The first phase involved optimization of antiviral activity through independent variation of quadrants 1-4. The second phase involved the preparation of hybrid structures combining the best of these substituents. Further SAR studies and pharmacokinetic considerations led to the identification of N-(2-pyridyl)-N'-(5-bromo-2- pyridyl)-thiourea (62; LY300046 · HCl) as a candidate for clinical evaluation. LY300046 · HCl inhibits HIV-1 RT with an IC50 of 15 nM and in cell culture has an ED50 of 20 nM.

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