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METHYL 9-FLUORENYLIDENEACETATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146967-87-5

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146967-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146967-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 146967-87:
(8*1)+(7*4)+(6*6)+(5*9)+(4*6)+(3*7)+(2*8)+(1*7)=185
185 % 10 = 5
So 146967-87-5 is a valid CAS Registry Number.

146967-87-5SDS

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 methyl 2-fluoren-9-ylideneacetate

1.2 Other means of identification

Product number -
Other names methyl 2-(9H-fluoren-9-ylidene)acetate

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:146967-87-5 SDS

146967-87-5Downstream Products

146967-87-5Relevant academic research and scientific papers

Modular Tandem Mizoroki-Heck/Reductive Heck Reactions to Construct Fluorenes from Cyclic Diaryliodoniums

Peng, Xiaopeng,Yang, Yang,Luo, Bingling,Wen, Shijun,Huang, Peng

supporting information, p. 222 - 226 (2020/12/01)

Starting from cyclic diaryliodoniums and terminal alkenes, a diverse set of fluorenes is conveniently constructed. The reactions catalyzed by palladium undergo one conventional Mizoroki-Heck reaction and one reductive Heck reaction. The scope of alkenes is general, leading to 29 fluorenes which would expand the structural diversity of fluorene reservoir. (Figure presented.).

Synthesis of 9-fluorenylidenes and 9,10-phenanthrenes through palladium-catalyzed aryne annulation by o-halostyrenes and o-halo allylic benzenes

Worlikar, Shilpa A.,Larock, Richard C.

supporting information; experimental part, p. 9132 - 9139 (2010/03/01)

(Chemical Equation Presented) A number of functionally substituted 9-fluorenylidenes and 9,10-phenanthrenes have been synthesized from substituted o-halostyrenes and o-halo allylic benzenes respectively in good yields by the palladium-catalyzed annulation

Esterification of amino acids and mono acids using triphosgene

Rivero,Heredia,Ochoa

, p. 2169 - 2175 (2007/10/03)

Alkyl esters of several amino acids and acids were prepared using triphosgene [trichloromethyl carbonate, TPA (2)].

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