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77103-90-3

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77103-90-3 Usage

Description

1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)is a chemical compound characterized by its molecular structure that features a tetrahydro-1-hydroxy-1-naphthalenyl group. 1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)is likely to exhibit some degree of aromaticity due to the presence of the naphthalenyl group. Although the specific properties and uses of this compound are not explicitly detailed, it may find applications in various sectors such as pharmaceuticals, dyes, or other industrial applications. Further testing and research are required to fully comprehend the potential applications and implications of 1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)-.

Uses

Used in Pharmaceutical Industry:
1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)is used as a potential compound for the development of new drugs in the pharmaceutical industry. Its unique molecular structure, which includes a naphthalenyl group, may offer novel therapeutic properties that can be harnessed for the treatment of various medical conditions.
Used in Dye Industry:
In the dye industry, 1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)may be utilized as a component in the synthesis of new dyes or pigments. 1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)-'s aromatic nature could contribute to the development of dyes with unique color characteristics and improved performance properties.
Used in Other Industrial Applications:
Beyond the pharmaceutical and dye industries, 1-(1,2,3,4-tetrahydro-1-hydroxy-1-naphthalenyl)may also find use in other industrial applications. Its specific properties and potential applications in these areas will depend on the results of further research and testing, which will help to elucidate the compound's full range of capabilities and potential benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 77103-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77103-90:
(7*7)+(6*7)+(5*1)+(4*0)+(3*3)+(2*9)+(1*0)=123
123 % 10 = 3
So 77103-90-3 is a valid CAS Registry Number.

77103-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-hydroxy-1,2,3,4-tetrahydronaphthalen-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(1-hydroxy-1,2,3,4- tetrahydronaphthalen-1-yl)ethanone

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:77103-90-3 SDS

77103-90-3Relevant articles and documents

Electroreductive acylation of aromatic ketones with acylimidazoles

Kise, Naoki,Agui, Syun,Morimoto, Shinji,Ueda, Nasuo

, p. 9407 - 9410 (2007/10/03)

The intermolecular reductive coupling of aromatic ketones with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-trimethylsiloxy ketones and esters. The best result was obtained using Bu4NPF6 as a supporting electrolyte and a Pb cathode in THF. The α-trimethylsiloxy-containing products were transformed to the corresponding α-hydroxy ketones and esters by treatment with TBAF in THF. This method was also effective for the intramolecular reductive coupling of δ- and ε-keto acylimidazoles.

Hypolipidemic 4,5-Dihydro-4-oxo-5,5-disubstituted-2-furancarboxylic Acids

Jirkovski, Ivo,Cayen, Mitchell, N.

, p. 1154 - 1156 (2007/10/02)

A series of novel 4,5-dihydro-4-oxo-5,5-disubstituted-2-furancarboxylic acids was synthesized and shown to possess potent hypotriglyceridemic activity in normal rats.In contrast to clofibrate, none of the present compounds altered liver weight at any dose

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