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

66045-88-3

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66045-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66045-88-3 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 66045-88:
(7*6)+(6*6)+(5*0)+(4*4)+(3*5)+(2*8)+(1*8)=133
133 % 10 = 3
So 66045-88-3 is a valid CAS Registry Number.

66045-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names E-2-(3'-fluorobenzylidene)-1-tetralone

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:66045-88-3 SDS

66045-88-3Downstream Products

66045-88-3Relevant academic research and scientific papers

Copper/GanPhos-Catalyzed 1,3-Dipolar Cycloaddition of Azo?-methine Ylides: An Efficient Access to Chiral Pyrrolidine Spirocycles

Gan, Zhenjie,Li, Ke,Zhang, Hui,Li, Er-Qing

supporting information, p. 1331 - 1340 (2020/11/30)

A highly efficient copper/GanPhos-catalyzed 1,3-dipolar cyclo?-addition?-of azomethine ylides is reported. This viable transformation provides a series of optically active spiro[dihydronaphthalene-2,3′-pyrrolidine]s, bearing one spiro quaternary and three tertiary stereogenic centers, in good yields and with high ee values. This protocol features high diastereo- A nd enantioselectivity, broad substrate scope and mild reaction conditions.

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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