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4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is a chemical compound characterized by its molecular formula C10H11NO5. It is a yellow crystalline solid that plays a significant role in the synthesis of various organic compounds, particularly in the production of pharmaceuticals, dyes, and other fine chemicals. Known for its aromatic properties, it is also utilized in the manufacturing of perfumes and flavorings. However, due to potential health risks and environmental hazards, careful handling of 4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is essential.

34837-88-2

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34837-88-2 Usage

Uses

Used in Pharmaceutical Industry:
4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and enhance the properties of existing ones.
Used in Dye Industry:
In the dye industry, 4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is used as a key component in the production of various dyes, contributing to the coloration and stability of these products.
Used in Perfume and Flavoring Industry:
4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is used as a raw material in the manufacturing of perfumes and flavorings, leveraging its aromatic properties to create unique scents and tastes.
Used in Fine Chemicals Industry:
4-METHOXY-3-NITRO-BENZENEACETIC ACID METHYL ESTER is also utilized in the production of fine chemicals, where its versatility in synthesis allows for the creation of specialized chemical products with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34837-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,3 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 34837-88:
(7*3)+(6*4)+(5*8)+(4*3)+(3*7)+(2*8)+(1*8)=142
142 % 10 = 2
So 34837-88-2 is a valid CAS Registry Number.

34837-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(4-methoxy-3-nitrophenyl)acetate

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid,4-methoxy-3-nitro-,methyl ester

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:34837-88-2 SDS

34837-88-2Relevant academic research and scientific papers

PYRAZOLE-OXAZOLIDINONE COMPOUND FOR ANTI-HEPATITIS B VIRUS

-

, (2019/06/07)

The present invention discloses a pyrazole-oxazolidinone compound having anti-hepatitis B virus activity, which has the structure of formula (I), wherein each variable is as defined herein.

SUBSTITUTED HETEROCYCLIC ACETAMIDES AS KAPPA OPIOID RECEPTOR (KOR) AGONISTS

-

, (2013/09/26)

The present invention relates to a series of substituted compounds having the general formula (I), including their ste reoisomers and/or their pharmaceutically acceptable salts, wherein R1, R2, R3. R4, R5, and R6 are as defined herein. This invention also relates to methods of making these compounds including intermediates. The compounds of this invention are effective at the kappa (κ) opioid receptor (KOR) site. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic pain, and associated disorders, particularly functioning peripherally at the CNS.

COMPOUNDS AND METHODS

-

, (2013/03/26)

The present invention relates to novel retinoid-related orphan receptor gamma (RORγ) modulators and their use in the treatment of diseases mediated by RORy.

Inhibitors of phospholipase enzymes

-

, (2008/06/13)

This invention provides substituted indole and indoline compounds useful in inhibiting phospholipase activity, particularly including cytosolic phospholipase A2 (cPLA2) activity, as well as pharmaceutical compositions containing the compounds and methods of using them to treat various maladies, including pain and inflammatory conditions.

Benzoxazepinones and their use as squalene synthase inhibitors

-

, (2008/06/13)

There is disclosed a compound represented by the formula [I]: wherein R1 is optionally substituted 1-carboxyethyl group, optionally substituted alkyl-sulfonyl group, optionally substituted (carboxy-cycloalkyl)-alkyl group, -X1-X2-Ar-X3-X4-COOH (wherein X1 and X4 are a bond or alkylene group, X2 and X3 are a bond, -O-, -S-, Ar is divalent aromatic group etc.), R2 is alkyl group optionally substituted with alkanoyloxy group and/or hydroxy group, R3 is alkyl group, and W is halogen atom, etc., or a salt thereof. The compound has the cholesterol lowering activity and the triglyceride lowering activity and is useful for preventing and/or treating hyperlipidemia.

SECONDARY METABOLITES OF Pyricularia oryzae. I. o-NITROPHENOL DERIVATIVES

Sviridov, S. I.,Ermolinskii, B. S.

, p. 691 - 696 (2007/10/02)

o-Nitrophenol derivatives have been isolated from the culture liquid of the deuteromycete Pyricularia oryzae Cav.: 4-hydroxy-3-nitrophenylacetic acid, 4-hydroxy-3-nitrobenzyl alcohol, 1- and 2-(4-hydroxy-3-nitrophenyl)ethanols, N-(4-hydroxy-3-nitrophenylethyl)acetamide, and pyriculamide.This is the first time that any of these compounds has been isolated from natural sources.The o-nitrophenols obtained possess moderate growth-inhibiting activity in relation to rice shoots.

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