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4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL, also known as 2-(thiophen-2-ylmethylamino)phenol, is a phenolic compound with the molecular formula C12H11NOS. It features a thiophen-2-ylmethyl group attached to the amino group on the phenol ring, endowing it with potential pharmacological properties. This versatile chemical is commonly utilized in organic synthesis and pharmaceutical research.

3139-28-4

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3139-28-4 Usage

Uses

Used in Pharmaceutical Research:
4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL is used as a research compound for its potential pharmacological properties, including its anti-inflammatory and analgesic effects. It is valued for its ability to modulate serotonin and dopamine receptors in the brain, which could have implications for the treatment of various neurological and psychiatric disorders.
Used in Organic Synthesis:
In the field of organic synthesis, 4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL is used as a building block or intermediate in the creation of more complex organic molecules, potentially leading to the development of new pharmaceuticals and other chemical products.
Used in Antioxidant Applications:
4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL is used as an antioxidant agent due to its ability to combat oxidative stress, which is implicated in many diseases and aging processes. Its antioxidant properties make it a candidate for use in health supplements and in the preservation of various products.
Used in Antibacterial Applications:
In the field of microbiology, 4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL is used as an antibacterial agent, potentially serving in the development of new antimicrobial drugs or as a preservative in various products to prevent bacterial growth.
Used in Chemical Research:
4-[(THIOPHEN-2-YLMETHYL)-AMINO]-PHENOL is used as a research tool in chemical research to study the effects of different functional groups on the properties of phenolic compounds, contributing to the understanding of structure-activity relationships in chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3139-28-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3139-28:
(6*3)+(5*1)+(4*3)+(3*9)+(2*2)+(1*8)=74
74 % 10 = 4
So 3139-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NOS/c13-10-5-3-9(4-6-10)12-8-11-2-1-7-14-11/h1-7,12-13H,8H2

3139-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(thiophen-2-ylmethylamino)phenol

1.2 Other means of identification

Product number -
Other names <4-Hydroxy-phenyl>-<2>thienylmethyl-amin

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:3139-28-4 SDS

3139-28-4Downstream Products

3139-28-4Relevant articles and documents

SYNTHESIS AND STUDY OF THE LIGHT-STABILIZING ACTIVITY OF SOME DITHIOCARBAMATES THAT INCLUDE A HETEROAROMATIC RING

Gol'dfarb, Ya. L.,Ostapenko, E'. G.,Ivanov, V.B.,Efremkin, A. F.,Litvinov, V. P.

, p. 1148 - 1153 (2007/10/02)

A number of new dithiocarbamates of transition metals that contain thiophene, furan, benzothiophene, and benzoselenophene rings were synthesized.The compounds obtained were investigated as light stabilizers for polymers.It is shown that the effectiv

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