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2-AMINO-1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANOL is a chemical compound characterized by the molecular formula C10H13NO3. It is a benzodioxin derivative that features an amino group and an ethanol functional group. 2-AMINO-1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANOL may hold potential applications in the pharmaceutical industry and research and development. Due to the lack of specific information on its properties and potential hazards, it is crucial to handle 2-AMINO-1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANOL with caution and adhere to proper safety protocols. Further research and information are required to fully comprehend its characteristics and possible uses.

4384-99-0

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4384-99-0 Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANOL is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, including the benzodioxin core and functional groups, may contribute to the development of new drugs with specific therapeutic properties.
Used in Research and Development:
In the field of research and development, 2-AMINO-1-(2,3-DIHYDRO-BENZO[1,4]DIOXIN-6-YL)-ETHANOL serves as a valuable compound for exploring its chemical properties, reactivity, and potential applications. It may be utilized in the synthesis of novel compounds, the study of reaction mechanisms, and the development of new methodologies in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 4384-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4384-99:
(6*4)+(5*3)+(4*8)+(3*4)+(2*9)+(1*9)=110
110 % 10 = 0
So 4384-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c11-6-8(12)7-1-2-9-10(5-7)14-4-3-13-9/h1-2,5,8,12H,3-4,6,11H2

4384-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanol

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethanol

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:4384-99-0 SDS

4384-99-0Downstream Products

4384-99-0Relevant academic research and scientific papers

Synthesis of isoquinolines and tetrahydroisoquinolines as potential antitumour agents

Capilla,Romero,Pujol,Caignard,Renard

, p. 8297 - 8303 (2007/10/03)

The isoquinoline 17 and the tetrahydroisoquinoline 16 were synthesized from 2,3-dihydro-1,4-benzodioxin (1) by different synthetic strategies. Preparation of arylethylamines and their cyclization in Bischler-Napieralski conditions have been studied. Another approach to isoquinolines was based on the amination of the ketone 13 followed by cyclization in acidic media. The route via the amide 15 was found to be more successful with respect to both yield and ease of reaction.

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