Welcome to LookChem.com Sign In|Join Free

CAS

  • or

49841-22-7

Post Buying Request

49841-22-7 Suppliers

Recommended suppliersmore

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

49841-22-7 Usage

General Description

1-NAPHTHO[2,1-B]FURAN-2-YLETHANONE is a chemical compound with the formula C14H8O2. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. 1-NAPHTHO[2,1-B]FURAN-2-YLETHANONE is used in the synthesis of various pharmaceuticals and fine chemicals. It has been studied for its potential anti-cancer and anti-inflammatory properties. Additionally, it has shown potential as a fluorescent probe for detecting metal ions. The compound has a naphthofuran core with a ketone functional group, making it a versatile building block for the synthesis of more complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 49841-22-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,4 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49841-22:
(7*4)+(6*9)+(5*8)+(4*4)+(3*1)+(2*2)+(1*2)=147
147 % 10 = 7
So 49841-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O2/c1-9(15)14-8-12-11-5-3-2-4-10(11)6-7-13(12)16-14/h2-8H,1H3

49841-22-7SDS

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-benzo[e][1]benzofuran-2-ylethanone

1.2 Other means of identification

Product number -
Other names 2-acetylnaphtho[2,1-b]furan

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:49841-22-7 SDS

49841-22-7Relevant articles and documents

Synthesis and cytotoxic evaluation of α-methylene-γ-butyrolactone bearing naphthalene and naphtho[2,1-b]furan derivatives

Lee, Kuan-Han,Huang, Bor-Ruey

, p. 333 - 338 (2002)

Naphthalene α-methylene-γ-butyrolactones exhibits a unique cytotoxicity profile. They are highly cytostatic for leukaemia cancer cells but are not cytocidal. For almost all the solid tumours tested, they are both cytostatic and cytocidal. Substitution of a bromo atom on either naphthalene or both naphthalene and γ-phenyl moiety of the lactone enhanced potency while retaining the same cytotoxicity profile. The tricyclic naphtho[2,1-b]furan derivatives, prepared from 2-hydroxy-1-naphthaldehyde in an efficient pathway, also possess the same cytotoxicity profile.

TBAI/TBHP mediated oxidative cross coupling of ketones with phenols and carboxylic acids: Direct access to benzofurans

Santhosh Kumar,Ravikumar,Chinna Ashalu,Rajender Reddy

supporting information, p. 33 - 37 (2017/12/11)

TBAI/TBHP mediated oxidative cross coupling of phenols and carboxylic acids with ketones has been reported under metal-free, base free, solvent free conditions enabling environmentally benign synthesis of aryloxyketones, acyloxy ketones and benzofurans. Phenoxyketones and acyloxylcarbonyl compounds were synthesized in good to high yields, where as benzofurans were synthesized in moderate yields. This method is operationally simple, works under mild conditions, using commercially available as well as inexpensive TBAI and an oxidant TBHP.

Synthesis and biological activity of some 3,4-dihydro-4-(4-substituted aryl)-6-(naptho[2,1-b]furan-2-yl pyrimidine-2(1H)-one derivatives

Gaikwad, Sanjeevan S.,Suryawanshi, Venkat S.,Lohar, Kishan S.,Jadhav, Dhanaji V.,Shinde, Narayan D.

experimental part, p. 175 - 180 (2012/05/20)

A series of new oxopyrimidine were prepared by cyclocondensation route with various substituted chalcones in presence of alcoholic solution of potassium hydroxide at reflux temperature. The synthesized oxopyrimidine derivatives were characterized by means

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 49841-22-7