30433-93-3

Basic information

• Product Name: 1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE
• Synonyms: AKOS ISYA01277;OTAVA-BB 1038642;1-(2-thienyl)propan-2-amine(SALTDATA: FREE);ASINEX-REAG BAS 10145056;1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE;RARECHEM AN KC 0145;TIMTEC-BB SBB010287;1-(2-THIENYL)PROPAN-2-AMINE
• CAS NO: 30433-93-3
• Molecular Formula: C7H11NS
• Molecular Weight: 141.23
• Mol File: 30433-93-3.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 210.8°C at 760 mmHg
• Flash Point: 81.3°C
• Appearance: /
• Density: 1.067g/cm³
• Vapor Pressure: 0.188mmHg at 25°C
• Refractive Index: 1.552
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE(30433-93-3)
• EPA Substance Registry System: 1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE(30433-93-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 30433-93-3(Hazardous Substances Data)

Usage

General Description

1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE, also known as 2-(2-Aminobenzyl)thiophene, is a chemical compound with the molecular formula C11H13NS. It is a yellow to brown liquid with a strong odor, and is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It is classified as an amine, with a thiophene ring and a methyl group attached to the amino group. 1-METHYL-2-THIOPHEN-2-YL-ETHYLAMINE has a variety of industrial and research applications, and its reactivity and unique structural properties make it a valuable tool in organic chemistry and drug development.

InChI:InChI=1/C7H11NS/c1-6(8)5-7-3-2-4-9-7/h2-4,6H,5,8H2,1H3

Upstream product

• 15022-18-1 1-(thiophen-2-yl)propan-2-one 
• 37629-59-7 (E)-2-(2-nitroprop-1-en-1-yl)thiophene 
• 6937-35-5 2-(2-nitroprop-1-enyl)thiophene 
• 98-03-3 thiophene-2-carbaldehyde 
• 23229-68-7 2-(prop-1-en-1-yl)thiophene 
• 20849-87-0 2-allylthiophene 
• 7664-41-7 ammonia 

Relevant articles and documents

Guanidine-containing compound as well as preparation method and application thereof

The invention discloses a cyanoguanidine-containing compound as well as a preparation method and application thereof. The invention also discloses a composition containing the cyanoguanidine-structured compound (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. The invention also discloses application thereof in preparation of analgesic drugs. The compounds of the invention are useful in the treatment of various pain.

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

CARBOXYLIC ACID AMIDES AS FACTOR XA INHIBITORS

The present invention relates to new substituted carboxylic acid amides of general formula (I), wherein D, B, R3, R4 and R5 are defined as in the specification, the tautomers, the enantiomers, the diastereomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, which have valuable properties.