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Benzoic acid, 3-hydroxy-4-methoxy-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71489-74-2

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71489-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71489-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,8 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71489-74:
(7*7)+(6*1)+(5*4)+(4*8)+(3*9)+(2*7)+(1*4)=152
152 % 10 = 2
So 71489-74-2 is a valid CAS Registry Number.

71489-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-4-methoxy-2-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Nitro-3-hydroxy-4-methoxy-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:71489-74-2 SDS

71489-74-2Relevant academic research and scientific papers

Preparation method of 3-hydroxy-4-methoxy-2-nitrobenzoic acid

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Paragraph 0050-0057; 0062-0064; 0069-0070, (2020/07/12)

The invention discloses a preparation method of 3-hydroxy-4-methoxy-2-nitrobenzoic acid, and belongs to the field of synthesis of medical intermediates. The preparation method comprises the followingsteps: starting from 3-alkoxy-4-acetoxybenzaldehyde (1), carrying out a nitration reaction process to obtain an intermediate (2), removing acetyl from the intermediate (2) to obtain an intermediate (3), methylating to obtain an intermediate (4), oxidizing the intermediate (4) to obtain an intermediate (5), deprotecting the intermediate (5), and recrystallizing to remove the isomer, thereby obtaining the 3-hydroxy-4-methoxy-2-nitrobenzoic acid (6). The method is simple, convenient and stable to operate, high in yield, environment-friendly, low in production cost and suitable for industrial large-scale production, and products in all steps are easy to separate.

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