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1(2H)-Naphthalenone, 2-[(2-fluorophenyl)methylene]-3,4-dihydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66045-87-2

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66045-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66045-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,4 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66045-87:
(7*6)+(6*6)+(5*0)+(4*4)+(3*5)+(2*8)+(1*7)=132
132 % 10 = 2
So 66045-87-2 is a valid CAS Registry Number.

66045-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-fluorophenyl)methylidene]-3,4-dihydronaphthalen-1-one

1.2 Other means of identification

Product number -
Other names 1(2H)-Naphthalenone,2-[(2-fluorophenyl)methylene]-3,4-dihydro

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:66045-87-2 SDS

66045-87-2Downstream Products

66045-87-2Relevant academic research and scientific papers

Basic Anion-Exchange Resin-Catalyzed Aldol Condensation of Aromatic Ketones with Aldehydes in Continuous Flow

Laroche, Benjamin,Saito, Yuki,Ishitani, Haruro,Kobayashi, Shū

supporting information, p. 961 - 967 (2019/05/02)

A general method for the aldol condensation of aromatic ketones with aldehydes was developed under continuous-flow conditions using a commercially available, strongly basic anion-exchange resin (A26) as catalyst. This procedure, in addition to exhibiting a wide substrate scope, promoted carbon-carbon bond formation under mild conditions using a quasi-stoichiometric ratio of starting reagents with good to excellent yields, thereby forming a limited amount of waste and allowing the process to be applied to sequential-flow systems. A proof of concept was developed in the first fully heterogeneously catalyzed two-step flow synthesis of donepezil, which is a blockbuster commercial anti-Alzheimer's drug.

E-2-benzylidenebenzocycloalkanones. Stereostructure and NMR spectroscopic investigation

Perjesi,Nusser,Tarczay, Gy.,Sohar

, p. 13 - 19 (2007/10/03)

Series of E-2-benzylideneindanones (a), -tetralones (b) and - benzosuberones (c) with OCH3 (2-4), NO2 (5-7) and F (8-10) substitutions (ortho, meta and para) on their benzylidene moiety were synthesized by aldol condensation of the a

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