Welcome to LookChem.com Sign In|Join Free
  • or
4-hydroxy-3-methyl-4-phenyl-1,3-thiazolidine-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19975-60-1

Post Buying Request

19975-60-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

19975-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19975-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,7 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19975-60:
(7*1)+(6*9)+(5*9)+(4*7)+(3*5)+(2*6)+(1*0)=161
161 % 10 = 1
So 19975-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NOS2/c1-11-9(13)14-7-10(11,12)8-5-3-2-4-6-8/h2-6,12H,7H2,1H3

19975-60-1SDS

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 4-hydroxy-3-methyl-4-phenyl-1,3-thiazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 2-Thiazolidinethione,4-hydroxy-3-methyl-4-phenyl

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:19975-60-1 SDS

19975-60-1Relevant academic research and scientific papers

Three-component and one-pot reaction between phenacyl bromide and primary amines in the presence of carbon disulfide

Hassanabadi, Alireza,Khandan-Barani, Khatereh

, p. 71 - 72 (2013/04/23)

A three-component and one-pot reaction between phenacyl bromide and primary amines in the presence of carbon disulfide to afford substituted 4-hydroxy-4-phenylthiazolidine-2-thiones in high yields.

Synthesis and Evaluation of 2(3H)-Thiazole Thiones as Tyrosinase Inhibitors

Emami, Saeed,Hosseinimehr, Seyed Jalal,Shahrbandi, Kami,Enayati, Ahmad Ali,Esmaeeli, Zahra

experimental part, p. 629 - 637 (2012/09/22)

A series of 2(3H)-thiazole thiones 3-5 was synthesized and evaluated for tyrosinase inhibition and DPPH radical scavenging activities. Among them, 3-methyl-4-phenyl-2(3H)-thiazole thione (4a) showed good tyrosinase inhibitory activity, even better than that of the well-known tyrosinase inhibitor, namely, kojic acid. From the structure-activity point of view, although it was found that the phenolic hydroxyl group in prototype 3-5 might contribute to the scavenging activity against DPPH radicals, there was no correlation between the potency of tyrosinase inhibition and the presence of the phenolic moiety. The in silico ADME-Tox screening revealed that the drug-likeness and drug-score values of the most potent compound 4a were significantly higher than those of kojic acid. Copyright

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 19975-60-1