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2,3,5,6-tetramethyl-4-nitrobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86145-89-3

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86145-89-3 Usage

General Description

2,3,5,6-tetramethyl-4-nitrobenzoic acid is a chemical compound with the molecular formula C11H11NO4. It is a yellow crystalline powder that is primarily used as a reagent in organic synthesis and as a pH indicator. 2,3,5,6-tetramethyl-4-nitrobenzoic acid is commonly used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various drugs and pesticides. Additionally, it is also used in the production of dyes and pigments. The chemical properties of 2,3,5,6-tetramethyl-4-nitrobenzoic acid make it a versatile compound for use in a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 86145-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,4 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86145-89:
(7*8)+(6*6)+(5*1)+(4*4)+(3*5)+(2*8)+(1*9)=153
153 % 10 = 3
So 86145-89-3 is a valid CAS Registry Number.

86145-89-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetramethyl-4-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Nitro-2,3,5,6-tetramethyl-benzoesaeure

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:86145-89-3 SDS

86145-89-3Relevant academic research and scientific papers

Regioselective Side-Chain Nitration of Polymethylbenzenes Directed by an Acyl Function and Its Application to the Synthesis of Polysubstituted Phthalic Acid Derivatives

Keumi, Takashi,Morita, Toshio,Teramoto, Koichi,Takahashi, Hisakazu,Yamamoto, Hiroshi,et al.

, p. 3439 - 3446 (2007/10/02)

Nitration of three types of tetramethylacetophenones and pentamethylacetophenone with fuming nitric acid in acetic anhydride was carried out.The product distributions were compared with those estimated from substituent effects.A variety of acylpentamethylbenzenes including pentamethylbenzoic acid were reacted with the nitrating system to give regioselectively 2-(nitromethyl)-3,4,5,6-tetramethylacylbenzenes.The selective nitrations of some benzoic acid derivatives followed by an alkaline treatment have been found to provide the N-hydroxyphthalimide derivatives, which a re readily converted to the phthalic anhydrides and the phthalazines.

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