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Phenanthren-9-yl acetate is an organic compound with the chemical formula C18H14O2. It is a derivative of phenanthrene, a polycyclic aromatic hydrocarbon, with an acetate group attached to the 9th carbon atom. phenanthren-9-yl acetate is characterized by its aromatic structure and ester functional group, which contributes to its chemical reactivity and properties. Phenanthren-9-yl acetate is often used in chemical research and synthesis, particularly in the preparation of various phenanthrene derivatives. It is also known for its potential applications in the pharmaceutical and materials science industries, where its unique structure can be exploited for specific purposes.

957-82-4

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957-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957-82-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 957-82:
(5*9)+(4*5)+(3*7)+(2*8)+(1*2)=104
104 % 10 = 4
So 957-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O2/c1-11(17)18-16-10-12-6-2-3-7-13(12)14-8-4-5-9-15(14)16/h2-10H,1H3

957-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name phenanthren-9-yl acetate

1.2 Other means of identification

Product number -
Other names 4-Acetoxyphenanthren

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:957-82-4 SDS

957-82-4Downstream Products

957-82-4Relevant academic research and scientific papers

Bay-Region Annulative π-Extension of o-Iodobiphenyls with Aliphatic Anhydrides Catalyzed by Pd(OAc)2

Huang, Lin,Chen, Li-Ping,Du, Yu,Fang, Mao-Ying,Wang, Bi-Qin,Feng, Chun,Xiang, Shi-Kai

supporting information, p. 7535 - 7539 (2021/10/12)

Bay-region annulative π-extension of o-iodobiphenyls with aliphatic anhydrides was developed. Many o-iodobiphenyls and aliphatic anhydrides can react well under the optimized conditions. A lot of phenanthrol derivatives can be efficiently prepared by this approach. The control experiments support that dibenzopalladacyclopentadienes may be the reaction intermediates.

Light-induced carbocyclization of iodoalkenes

Campos-Gómez, Esther,Campos, Pedro J.,González, Héctor F.,Rodríguez, Miguel A.

experimental part, p. 4292 - 4295 (2012/07/16)

The direct irradiation of iodoalkenes leads to the formation of carbon-centered radical by homolysis of the C-I bond. The photoreaction is used in cyclizations with formation of six membered rings.

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