Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15386-52-4

Post Buying Request

15386-52-4 Suppliers

Recommended suppliersmore

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

15386-52-4 Usage

Structure

A derivative of 1,2-benzenediol with a thiazole ring and an amino group at the 2-position.

Biological activity

Potential biological activity, which may be useful in pharmaceutical research or drug development.

Structural features

Thiazole ring and amino group at the 2-position contribute to the compound's potential pharmacological properties.

Further research

Additional study may be needed to fully understand the potential uses and effects of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 15386-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,8 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15386-52:
(7*1)+(6*5)+(5*3)+(4*8)+(3*6)+(2*5)+(1*2)=114
114 % 10 = 4
So 15386-52-4 is a valid CAS Registry Number.

15386-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-amino-1,3-thiazol-4-yl)benzene-1,2-diol

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:15386-52-4 SDS

15386-52-4Relevant articles and documents

An efficient strategy for protecting dihydroxyl groups of catechols

Huang, Wei-Bin,Guo, Ying,Jiang, Jian-An,Pan, Xian-Dao,Liao, Dao-Hua,Ji, Ya-Fei

, p. 741 - 746 (2013/05/09)

A novel strategy for protecting dihydroxyl groups of catechols has been developed. Base-mediated cyclizations of catechols with 1,3-dibromopropane provided the corresponding benzo[b]1,4-dioxepans, and herefrom the protecting group was easily cleaved by aluminum chloride. The preparation of the antibacterial and antifungal agent 4-(2-aminothiazol-4-yl)benzene-1,2-diol from catechol reliably verified its availability amenable to various harsh reaction conditions. Georg Thieme Verlag Stuttgart - New York.

Synthesis of some new 4-{2-[(aryl)amino]-1,3-thiazol-4-yl}benzene-1,2-diols as possible antibacterial and antifungal agents

Narayana,Ashalatha,Vijaya Raj,Suchetha Kumari

, p. 1381 - 1389 (2007/10/03)

Some new 4-{2-[(aryl) amino]-1,3-thiazol-4-yl}benzene-1,2-diols are prepared and characterized by spectral analysis. The newly prepared compounds are studied for their antibacterial and antifungal activity. Interestingly, almost all the compounds are found to possess promising antibacterial and antifungal activity against all tested microorganisms. Copyright Taylor & Francis Group, LLC.

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

What can I do for you?
Get Best Price

Get Best Price for 15386-52-4