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4-(2-Methoxyethoxy)aniline, also known as Dimethoxyethylphenylamine or DMEP, is a chemical compound with the molecular formula C9H13NO2. It is a pale yellow to brown liquid at room temperature and is characterized by its various functional groups, making it a versatile compound for a range of chemical reactions. It is commonly used in industrial applications as a solvent, intermediate, or additive, and is also utilized in the production of dyes, pharmaceuticals, and other organic compounds.

33311-29-4

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33311-29-4 Usage

Uses

Used in Chemical Industry:
4-(2-Methoxyethoxy)aniline is used as a solvent for various chemical reactions due to its ability to dissolve a wide range of substances and facilitate reaction processes.
Used in Pharmaceutical Industry:
4-(2-Methoxyethoxy)aniline is used as an intermediate in the synthesis of pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Dye Production:
4-(2-Methoxyethoxy)aniline is used as a key component in the production of dyes, providing color and stability to various products.
Used in Organic Compound Synthesis:
4-(2-Methoxyethoxy)aniline is used as a building block in the synthesis of other organic compounds, leveraging its functional groups to create a diverse range of molecules with specific properties and applications.
It is important for researchers and chemists to understand the properties and applications of 4-(2-Methoxyethoxy)aniline in order to utilize it effectively and safely in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 33311-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33311-29:
(7*3)+(6*3)+(5*3)+(4*1)+(3*1)+(2*2)+(1*9)=74
74 % 10 = 4
So 33311-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO2/c1-11-6-7-12-9-4-2-8(10)3-5-9/h2-5H,6-7,10H2,1H3

33311-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-METHOXYETHOXY)ANILINE

1.2 Other means of identification

Product number -
Other names 4-Methoxyaethoxy-anilin

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:33311-29-4 SDS

33311-29-4Relevant academic research and scientific papers

S-triazine compounds as well as preparation method and application thereof

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Paragraph 0088-0090, (2020/05/05)

The invention discloses s-triazine compounds and pharmaceutically acceptable salts thereof; experiments prove that the compounds can be used for treating or preventing diseases related to protein kinase activity, such as leukemia and lymphoma, by inhibiti

As tyrosine kinase inhibitors containing nitrogen and ring compound

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Paragraph 0313; 0314; 0315; 0316, (2017/04/26)

The invention belongs to the technical field of medicine, particularly relates to a heterocyclic nitrogen compound which acts as a tyrosine kinase inhibitor and is represented by a general formula (I) as well as a deuterated material, pharmaceutically acc

ARYL SULFONAMIDE COMPOUNDS AS CARBONIC ANHYDRASE INHIBITORS AND THEIR THERAPEUTIC USE

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Page/Page column 67, (2017/01/23)

Disclosed herein are compounds having the following structure useful as inhibitors of carbonic anhydrase IX (CAIX) and XII, and particularly useful for reducing or eliminating metastases see Formula (I).

PROPENAMIDE THIOPHENE DERIVATIVES AS FLAVIVIRUS INHIBITORS AND THEIR USE

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Page/Page column 24, (2017/07/06)

The present invention deals with new flavivirus inhibitors, compositions comprising said inhibitors and methods for the treatment of disorders related to a viral infection, such as a disease due to a flavivirus infection, comprising administering said inhibitors.

Eeyarestatin I derivatives with improved aqueous solubility

Ding, Rui,Zhang, Ting,Xie, Jiashu,Williams, Jessica,Ye, Yihong,Chen, Liqiang

supporting information, p. 5177 - 5181 (2016/11/09)

Inhibition of p97 (also known as valosin-containing protein (VCP)), has been validated as a promising strategy for cancer therapy. Eeyarestatin I (EerI) blocks p97 through a novel mechanism of action and has favorable anti-cancer activities against cultured cancer cells. However, its poor aqueous solubility severely limits its in vivo applications. To circumvent this problem, we have identified EerI derivatives that possess improved aqueous solubility by introducing a single solubilizing group. These modified compounds preserved endoplasmic reticulum (ER) stress-inducing and antiproliferative activities as well as generally good in vitro metabolic properties, suggesting that these EerI derivatives could serve as candidates for further optimization.

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 00768; 00770, (2015/09/28)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

HETEROCYCLIC COMPOUNDS AND USES THEREOF

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Paragraph 00243; 00245, (2015/02/02)

The present invention relates to pharmaceutical compounds, compositions and methods, especially as they are related to compositions and methods for the treatment and/or prevention of a proliferation disorder, a cancer, a tumor, an inflammatory disease, an autoimmune disease, psoriasis, dry eye or an immunologically related disease, and in some embodiments diseases or disorders related to the dysregulation of kinase such as, but not limited to, EGFR (including HER), Alk, PDGFR, BLK, BMX/ETK, FLT3(D835Y), ITK, TEC, TXK, BTK, or JAK, and the respective pathways.

INHIBITORS OF BRUTON'S TYROSINE KINASE

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Paragraph 00544; 00547, (2014/09/03)

Disclosed herein are compounds that form covalent bonds with Bruton's tyrosine kinase (Btk). Also described are irreversible inhibitors of Btk. In addition, reversible inhibitors of Btk are also described. Also disclosed are pharmaceutical compositions th

ALKYLQUINOLINE AND ALKYLQUINAZOLINE KINASE MODULATORS

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Page/Page column 72, (2010/11/25)

The invention is directed to alkylquinoline and alkylquinazoline compounds of Formula I: wherein R1, R2, R3, B, Z, G, Q and X are as defined herein, the use of such compounds as protein tyrosine kinase modulators, particularly inhibitors of FLT3 and/or c-kit and/or TrkB, the use of such compounds to reduce or inhibit kinase activity of FLT3 and/or c-kit and/or TrkB in a cell or a subject, and the use of such compounds for preventing or treating in a subject a cell proliferative disorder and/or disorders related to FLT3 and/or c-kit and/or TrkB. The present invention is further directed to pharmaceutical compositions comprising the compounds of the present invention and to methods for treating conditions such as cancers and other cell proliferative disorders.

Chemokine receptor binding compounds

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Page/Page column 17, (2008/06/13)

The present invention relates to chemokine receptor binding compounds, pharmaceutical compositions and their use. More specifically, the present invention relates to modulators of chemokine receptor activity, preferably modulators of CCR5. These compounds

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