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3-(2-methoxyethoxy)aniline hydrochloride is a chemical compound with the molecular formula C8H12ClNO2. It is a hydrochloride salt derivative of 3-(2-methoxyethoxy)aniline, known for its versatility in chemical and pharmaceutical applications.

110178-35-3

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110178-35-3 Usage

Uses

Used in Chemical Synthesis:
3-(2-methoxyethoxy)aniline hydrochloride is used as an intermediate in the synthesis of other organic compounds, contributing to the formation of various chemical products.
Used in Dyes and Pigments Production:
3-(2-methoxyethoxy)aniline hydrochloride is used as a component in the production of dyes and pigments, providing coloration properties to different materials.
Used in Pharmaceutical Manufacturing:
3-(2-methoxyethoxy)aniline hydrochloride is used in the manufacturing of medications and pharmaceuticals, playing a role in the development of new drugs and therapies.
Used in Research and Development:
3-(2-methoxyethoxy)aniline hydrochloride is utilized in research and development settings, where it aids in the exploration of new chemical reactions and the advancement of scientific knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 110178-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,7 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110178-35:
(8*1)+(7*1)+(6*0)+(5*1)+(4*7)+(3*8)+(2*3)+(1*5)=83
83 % 10 = 3
So 110178-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO2/c1-11-5-6-12-9-4-2-3-8(10)7-9/h2-4,7H,5-6,10H2,1H3

110178-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Methoxyethoxy)aniline

1.2 Other means of identification

Product number -
Other names -

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:110178-35-3 SDS

110178-35-3Relevant academic research and scientific papers

FLUOROALLYLAMINE DERIVATIVE AND USE THEREOF

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Paragraph 0346, (2020/03/17)

The present invention relates to a fluoroallylamine derivative and use thereof. In particular, the present invention relates to a compound as shown in Formula I, a prodrug, an isomer, an isotope-labeled compound, a solvate or a pharmaceutically acceptable salt thereof, which has VAP-1/SSAO inhibitory activity, and can be used for treating a disease associated with VAP-1/SSAO overactivity.

SUBSTITUTED AROMATIC SULFUR COMPOUNDS AND METHODS OF THEIR USE

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Page/Page column 62-63, (2012/09/11)

Compounds of formula II are described, wherein D, n, Ra, Rb, and Rc are as herein defined, along with pharmaceutical compositions and methods of using compounds of formula II for treating or reducing the risk of peritoneal carcinomatosis in a patient.

UREA SUBSTITUTED SULPHONAMIDE DERIVATIVES

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Page/Page column 66; 69, (2010/12/31)

The present invention relates to sulphonamide derivatives, whith a urea moiety. The invention also relates to the use of the derivatives as inhibitors of collagen receptor integrins, especially α2β1 integrin inhibitors e.g. in connection with diseases and

Vanilloid receptor ligands and their use in treatments

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, (2008/06/13)

Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritis, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

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