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17056-93-8

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17056-93-8 Usage

Description

1-(3-Hydroxynaphthalen-2-Yl)Ethanone, a chemical compound with the molecular formula C12H10O2, is a yellowish-brown solid that is widely utilized in the chemical and pharmaceutical industries. It features a naphthalene ring with a hydroxyl group and a ketone functional group attached, which contributes to its diverse applications.

Uses

Used in Pharmaceutical Industry:
1-(3-Hydroxynaphthalen-2-Yl)Ethanone is used as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity.
Used in Fragrance Industry:
1-(3-Hydroxynaphthalen-2-Yl)Ethanone is used as a key component in the creation of fragrances, capitalizing on its chemical properties to produce distinct and appealing scents.
Used in Dye Industry:
1-(3-Hydroxynaphthalen-2-Yl)Ethanone is employed as a starting material for the production of dyes, taking advantage of its chemical composition to generate a range of colors.
Used in Research and Development:
1-(3-Hydroxynaphthalen-2-Yl)Ethanone is used as a reagent in organic synthesis, facilitating the development of new chemical compounds and materials.
Used in Fluorescent Probes and Dyes:
Leveraging its fluorescent properties, 1-(3-Hydroxynaphthalen-2-Yl)Ethanone is used in the development of fluorescent probes and dyes for various applications, including biological imaging and detection.
Used in Anti-Inflammatory and Anti-Cancer Applications:
1-(3-Hydroxynaphthalen-2-Yl)Ethanone has been studied for its potential anti-inflammatory and anti-cancer properties, making it a promising candidate for further research and development in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 17056-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,5 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17056-93:
(7*1)+(6*7)+(5*0)+(4*5)+(3*6)+(2*9)+(1*3)=108
108 % 10 = 8
So 17056-93-8 is a valid CAS Registry Number.

17056-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-hydroxynaphthalen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(3-hydroxy-[2]naphthyl)-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:17056-93-8 SDS

17056-93-8Downstream Products

17056-93-8Relevant articles and documents

Molecular tweezers: Synthesis and formation of host-guest complexes

Legouin, Beatrice,Gayral, Maud,Uriac, Philippe,Cupif, Jean-Francois,Levoin, Nicolas,Toupet, Loic,Van De Weghe, Pierre

, p. 5503 - 5508 (2010)

A chiral molecular tweezer obtained from (+)-usnic acid placed in solution in the presence of various aromatic compounds afforded complexes with low association constants. Thus, the X-ray structure of assembly 31 is presented, where the guest is sandwiched between the two pincers of the tweezer. The association constants for various guests were determined through different methods. Finally, other tweezers with electron-rich aromatic aldehydes and ketones were prepared from (1R,2R)-1,2-diaminocyclohexane. The most interesting complexes were also confirmed through structural analysis, and the best results were obtained with 10-hydroxyphenanthrene-9-carbaldehyde (51) as the aromatic moiety.

Convenient Syntheses of Naturally Occurring Angular and Linear Naphthopvrans

Paradkar, Madhusudan V.,Godbole, Himanshu M.,Ranade, Anup A.,Joseph, Augustine R.

, p. 318 - 319 (1998)

A convenient synthesis of naturally occurring angular naphthopyrans and their 6-demethoxy derivatives is described starting from 2-acetyl-1-naphthols along with the synthesis of linear naphthopyrans from 3-acetyl-2-naphthol.

Solvatofluorochromic flavonoid dyes with enlarged transition dipole moments enable the ratiometric detection of methanol in commercial biodiesel with improved sensitivities

Du, Bing,Huang, Yingying,Liu, Bin,Qin, Tianyi,Xu, Hanhong,Xun, Zhiqing,Yao, Guangkai,Zhao, Chen

, p. 16808 - 16814 (2020/12/30)

Detection of methanol in commercial biodiesel is essential to evaluate the fuel quality associated with the matter of driving safety. Compared to the standard GC method, the fluorescent detection method for methanol is much simpler and faster, but still u

Synthesis of Polysubstituted 2-Naphthols by Palladium-Catalyzed Intramolecular Arylation/Aromatization Cascade

Cai, Jinhui,Hu, Xu-Dong,Liu, Wen-Bo,Wang, Zhen-Kai,Yao, Fei,Zhang, Yun-Hao

supporting information, (2020/02/25)

A palladium-catalyzed intramolecular α-arylation and defluorinative aromatization strategy for the synthesis of polysubstituted 2-naphthols is reported. With ortho-bromobenzyl-substituted α-fluoroketones as the substrates and palladium acetate/triphenylphosphine as the catalyst, this method features good functional group tolerance, readily available catalyst and starting materials, and high yields. The applications of the strategy are demonstrated by the synthesis of useful building blocks, such as naphtha[2,3-b]furan, naphthol AS-D, and ligands/catalysts. (Figure presented.).

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