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4-Nitro-3-tert-butylphenol is an organic compound characterized by its molecular formula C10H13NO3. It is a derivative of phenol, with a nitro group (-NO2) attached at the 4th carbon position and a tert-butyl group (-C(CH3)3) at the 3rd carbon position. This yellow crystalline solid is insoluble in water but soluble in organic solvents such as ethanol and ether. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other chemical products. Due to its reactivity and potential health hazards, it is important to handle 4-Nitro-3-tert-butylphenol with care, following proper safety protocols.

5722-68-9

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5722-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5722-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5722-68:
(6*5)+(5*7)+(4*2)+(3*2)+(2*6)+(1*8)=99
99 % 10 = 9
So 5722-68-9 is a valid CAS Registry Number.

5722-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-Butyl-4-nitrophenol

1.2 Other means of identification

Product number -
Other names 4-Nitro-3-tert-butylphenol

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:5722-68-9 SDS

5722-68-9Upstream product

5722-68-9Relevant academic research and scientific papers

STUDIES ON THE TWO-PHASE NITRATION OF SELECTED PHENOLS

Thompson, Malcolm J.,Zeegers, Petrus J.

, p. 2471 - 2474 (2007/10/02)

The two phase nitration of several phenols by aqueous acid, sodium nitrate and diethyl ether, yielded as well as the expected nitro-phenols, a benzoquinone.A variable induction period was observed which could be significantly reduced by added sodium nitrite.

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