Welcome to LookChem.com Sign In|Join Free

CAS

  • or

78119-82-1

Post Buying Request

78119-82-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

78119-82-1 Usage

Description

6-Hydroxy-2-naphthaldehyde is a chemical compound characterized by the chemical formula C11H8O2. It is a yellow solid that exhibits solubility in organic solvents while remaining insoluble in water. 6-Hydroxy-2-naphthaldehyde is distinguished by its unique chemical properties, which make it valuable for a range of applications in both industrial and research settings.

Uses

Used in Organic Synthesis:
6-Hydroxy-2-naphthaldehyde is utilized as a reagent in organic synthesis processes, particularly for the production of pharmaceuticals and dyes. Its chemical structure allows it to serve as a key intermediate in the synthesis of various organic compounds, contributing to the development of new and improved products in these industries.
Used in Research:
6-Hydroxy-2-naphthaldehyde has been the subject of research for its potential biological activities. Studies have explored its antioxidant properties, which could have implications for health and medicine. Additionally, it has been investigated for its potential use as a chemo-sensor, specifically for detecting metal ions. This capability could be applied in environmental monitoring, analytical chemistry, and other fields where the detection of specific metal ions is crucial.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Hydroxy-2-naphthaldehyde is used as a precursor for the synthesis of various pharmaceutical compounds. Its role in the development of new drugs is significant, as it can contribute to the creation of medications with novel mechanisms of action or improved therapeutic profiles.
Used in Dye Industry:
6-Hydroxy-2-naphthaldehyde is also used in the dye industry for the production of dyes. Its chemical properties make it suitable for the creation of dyes with specific color characteristics and stability, which are important for various applications, including textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 78119-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78119-82:
(7*7)+(6*8)+(5*1)+(4*1)+(3*9)+(2*8)+(1*2)=151
151 % 10 = 1
So 78119-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H8O2/c12-7-8-1-2-10-6-11(13)4-3-9(10)5-8/h1-7,13H

78119-82-1SDS

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 6-Hydroxy-2-naphthaldehyde

1.2 Other means of identification

Product number -
Other names 6-hydroxynaphthalene-2-carbaldehyde

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:78119-82-1 SDS

78119-82-1Upstream product

78119-82-1Relevant articles and documents

Stoichiometric Nitroxyl Photorelease Using the (6-Hydroxy-2-naphthalenyl)methyl Phototrigger

Zhou, Yang,Cink, Ruth B.,Seed, Alexander J.,Simpson, M. Cather,Sampson, Paul,Brasch, Nicola E.

, p. 1054 - 1057 (2019)

The design and synthesis of a photoactivatable HNO donor incorporating the (6-hydroxynaphthalen-2-yl)methyl (6,2-HNM) photocage coupled to the trifluoromethanesulfonamidoxy analogue of the well-established HNO generator Piloty's acid is described. The photoactive HNO donor stoichiometrically generates HNO (~98%) at neutral pH conditions, and evidence for concerted C-O and N-S bond cleavage was obtained. The methanesulfonamidoxy analogue primarily undergoes undesired N-O bond cleavage.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 78119-82-1