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2-tert-butyl-5-methyl-4-nitrosophenol is an organic compound characterized by its chemical formula C11H15NO2. It is a derivative of phenol, with a tert-butyl group at the 2-position, a methyl group at the 5-position, and a nitroso group at the 4-position. 2-tert-butyl-5-methyl-4-nitrosophenol is known for its potential applications in the synthesis of various organic compounds and may have uses in the pharmaceutical or chemical industries. Due to the presence of the nitroso group, it is important to handle 2-tert-butyl-5-methyl-4-nitrosophenol with care, as nitroso compounds can be reactive and may pose health risks.

5435-72-3

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5435-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5435-72-3 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, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5435-72:
(6*5)+(5*4)+(4*3)+(3*5)+(2*7)+(1*2)=93
93 % 10 = 3
So 5435-72-3 is a valid CAS Registry Number.

5435-72-3SDS

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 2-tert-butyl-5-methyl-4-nitrosophenol

1.2 Other means of identification

Product number -
Other names 2-tert-Butyl-5-methyl-4-nitroso-phenol

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:5435-72-3 SDS

5435-72-3Upstream product

5435-72-3Relevant academic research and scientific papers

Synthesis and antioxidant activity of thymol and carvacrol based Schiff bases

Beena,Kumar, Deepak,Rawat, Diwan S.

, p. 641 - 645 (2013/03/13)

Thymol and carvacrol are well known antioxidants found in the extract of the plants of thyme species. The Schiff bases of 2-iso-propyl-5-methyl-phenol (thymol/1a), 2-tert-butyl-5-methyl-phenol (1b) and 5-iso-propyl-2-methyl-phenol (carvacrol/1c) exhibited much better antioxidant activity than thymol and carvacrol in DPPH assay. Ten compounds (4k, 4l, 4r, 5k, 5l, 5q, 5r, 6k, 6l and 6r) showed better or similar activity as compared to the reference compound ascorbic acid. Twenty-four most active compounds were also screened by ABTS method and showed 60-90% inhibition at 5 μg/mL concentration.

TRICYCLIC DIHYDROBENZOFURAN DERIVATIVES, PROCESS FOR THE PREPARATION THEREOF AND AGENTS

-

, (2008/06/13)

A compound represented by the formula: wherein Ring A is a non-aromatic 5- to 7-membered nitrogen-containing heterocyclic ring which may be further substituted, Ring B is benzene ring which is further substituted, Ring C is a dihydrofuran ring which may b

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