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5435-28-9

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5435-28-9 Usage

Description

(3,4,5-trimethoxy-2-nitrophenyl)methanol, also known as TNNM, is a chemical compound with the molecular formula C10H13NO6. It is a substituted phenol derivative characterized by the presence of three methoxy groups and a nitro group attached to the aromatic ring. TNNM is recognized for its potential as a precursor in the synthesis of pharmaceuticals and organic compounds, as well as its utility in research and development for creating new molecules with possible medicinal or industrial applications.

Uses

Used in Pharmaceutical Synthesis:
TNNM is utilized as a precursor in the pharmaceutical industry for the synthesis of various drugs and organic compounds. Its unique structure allows it to be a versatile building block in the development of new medicinal agents.
Used in Research and Development:
In the realm of research and development, TNNM serves as a valuable component for the creation of novel molecules. Its properties make it suitable for exploring potential applications in medicine and industry, contributing to the advancement of scientific knowledge.
Used in Antioxidant and Anti-Inflammatory Applications:
Although further studies are required, TNNM may exhibit potential as an antioxidant and anti-inflammatory agent. Its chemical structure suggests it could play a role in combating oxidative stress and inflammation, which are important factors in various diseases and conditions.
Used in Industrial Applications:
Beyond its pharmaceutical and research applications, TNNM may also find use in various industrial processes. Its chemical properties could be harnessed for specific technical applications, although the exact uses would depend on the industry's needs and further research into its practical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5435-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5435-28:
(6*5)+(5*4)+(4*3)+(3*5)+(2*2)+(1*8)=89
89 % 10 = 9
So 5435-28-9 is a valid CAS Registry Number.

5435-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4,5-trimethoxy-2-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names 3,4,5-trimethoxy-2-nitrobenzyl methanol

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:5435-28-9 SDS

5435-28-9Relevant articles and documents

Synthesis of photocaged diamines and their application in photoinduced self-assembly

Barra, Tomas,Arrue, Lily,Urzúa, Esteban,Ratjen, Lars

, (2019/02/06)

The photochemical cleavage of covalent bonds is an important strategy in protection group chemistry, as well as for the triggering of chemical events posterior to the application of the physicochemical stimulus. Photocages allow the arresting and traceles

Concise syntheses of N-aryl-5,6,7-trimethoxyindoles as antimitotic and vascular disrupting agents: Application of the copper-mediated Ullmann-type arylation

Lee, Hsueh-Yun,Chang, Jang-Yang,Chang, Ling-Yin,Lai, Wen-Yang,Lai, Mei-Jung,Shih, Kuang-Hsing,Kuo, Ching-Chuan,Chang, Chi-Yen,Liou, Jing-Ping

supporting information; experimental part, p. 3154 - 3157 (2011/05/12)

In an attempt to mimic the 3,4,5-trimethoxyphenyl-Z-stilbene moiety of combretastatin A-4, a series of N-aryl-5,6,7-trimethoxyindoles were synthesized via copper-catalyzed Ullmann-type N-arylation through the corresponding 5,6,7-trimethoxyindole and aryl halides. These synthesized compounds demonstrated potent antiproliferative activity providing a novel skeleton for potent tubulin polymerization inhibitors.

2-Amino and 2′-aminocombretastatin derivatives as potent antimitotic agents

Chang, Jang-Yang,Yang, Ming-Fang,Chang, Chi-Yen,Chen, Chi-Ming,Kuo, Ching-Chuan,Liou, Jing-Ping

, p. 6412 - 6415 (2007/10/03)

A novel series of 2-amino and 2′-aminocombretastatin derivatives were synthesized and evaluated for antitumor activity. Several compounds had excellent antiproliferative activity as inhibitors of tubulin polymerization. Compounds 11, 20, and 21 with ICsu

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