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2-Amino-1-tetralone hydrochloride, also known as 1-amino-2-naphthalenone hydrochloride, is a crystalline solid with the chemical formula C10H11NO·HCl. It is a derivative of tetralone and is commonly used in the synthesis of pharmaceuticals and organic compounds. This versatile chemical is also utilized in research and laboratory settings as a reagent or intermediate in organic synthesis reactions. Due to its structural similarity to certain neurotransmitters and potential biological activity, 2-Amino-1-tetralone hydrochloride has applications in medicinal chemistry and drug discovery.

6298-95-9

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6298-95-9 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Amino-1-tetralone hydrochloride is used as a key intermediate in the synthesis of various pharmaceuticals, particularly for the development of new drugs and active pharmaceutical ingredients. Its unique structure allows for the creation of compounds with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic chemistry, 2-Amino-1-tetralone hydrochloride serves as a valuable reagent for the synthesis of a wide range of organic compounds. Its versatility in forming different chemical bonds and reactions makes it an essential component in various organic synthesis processes.
Used in Medicinal Chemistry and Drug Discovery:
2-Amino-1-tetralone hydrochloride is used as a structural template in medicinal chemistry for the design and development of new drugs. Its resemblance to neurotransmitters and potential biological activity make it a promising candidate for drug discovery, particularly in the areas of central nervous system disorders and other therapeutic applications.
Used in Insecticide Production:
As a derivative of tetralone, 2-Amino-1-tetralone hydrochloride is also used in the production of insecticides. Its chemical properties contribute to the development of effective insect control agents, which are essential for agricultural and environmental management.
Used in Fragrance Chemicals:
2-Amino-1-tetralone hydrochloride finds application in the fragrance industry due to its ability to contribute to the creation of unique and complex scents. Its use in the synthesis of fragrance chemicals allows for the development of novel and innovative perfumes and scented products.

Check Digit Verification of cas no

The CAS Registry Mumber 6298-95-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6298-95:
(6*6)+(5*2)+(4*9)+(3*8)+(2*9)+(1*5)=129
129 % 10 = 9
So 6298-95-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-4,9H,5-6,11H2

6298-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3,4-dihydro-2H-naphthalen-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-amino-3,4-dihydro-2H-1-naphthalenone hydrochloride

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:6298-95-9 SDS

6298-95-9Relevant academic research and scientific papers

Syntheses and Photophysical Properties of Some 5(2)-Aryl-2(5)-(4-pyridyl)oxazoles and Related Oxadiazoles and Furans

Hall, J. Herbert,Chien, Joseph Yuming,Kauffman, Joel M.,Litak, Peter T.,Adams, Jeffrey K.,et al.

, p. 1245 - 1273 (2007/10/02)

A number of 5-aryl-2-(4-pyridyl)oxazoles, a 2-aryl-5-(4-pyridyl)oxazole, the related oxadiazole and furan, several 2-(4-pyridyl)cycloalkanooxazoles, and many of their quaternary salts were prepared.No single standard synthesis was effective for preparation of more than a few of the 25 free bases described; methods often unique to a base were employed.Minor variations in structure sometimes produced large differences in absorption and emission wavelengths, as well as in the magnitude of the extinction coefficient.The salts are of interest as laser dyes, scintillation fluors, biological stains, and shifters for luminescent solar concentrators.

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