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"9(10H)-Phenanthrenone, 10-hydroxy-10-(phenylmethyl)-" is a complex organic compound with the molecular formula C20H16O2. It is a derivative of phenanthrene, a polycyclic aromatic hydrocarbon, with a ketone group at position 9 and a hydroxyl group at position 10, connected to a phenylmethyl group. 9(10H)-Phenanthrenone, 10-hydroxy-10-(phenylmethyl)- is characterized by its unique structure, which includes a phenanthrene core with a carbonyl group and a hydroxyl group, as well as a benzyl group attached to the hydroxyl-bearing carbon. It is a white crystalline solid and is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds due to its reactive functional groups. The compound's chemical properties and reactivity are influenced by the presence of the ketone, hydroxyl, and benzyl groups, which can participate in a range of chemical reactions, such as nucleophilic addition, oxidation, and substitution.

5025-29-6

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5025-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5025-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5025-29:
(6*5)+(5*0)+(4*2)+(3*5)+(2*2)+(1*9)=66
66 % 10 = 6
So 5025-29-6 is a valid CAS Registry Number.

5025-29-6SDS

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 10-benzyl-10-hydroxyphenanthren-9-one

1.2 Other means of identification

Product number -
Other names 9-Hydroxy-9-benzyl-10-oxo-9,10-dihydro-phenanthren

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:5025-29-6 SDS

5025-29-6Downstream Products

5025-29-6Relevant academic research and scientific papers

Photo-allylation and photo-benzylation of carbonyl compounds using organotrifluoroborate reagents

Nishigaichi, Yutaka,Orimi, Takayuki,Takuwa, Akio

experimental part, p. 3837 - 3839 (2010/03/04)

Allyl- and benzyl-trifluoroborates can be applied to the photoreaction of carbonyl compounds to afford the corresponding alcoholic adducts in acceptable yields via a photo-induced single electron transfer pathway. The results were confirmed from the react

Novel reactions of indium reagents with 1,2-diones: A facile synthesis of α-hydroxy ketones

Nair, Vijay,Jayan,Ros, Sindu

, p. 9453 - 9459 (2007/10/03)

Indium mediated reactions of allyl, cinnamyl, propargyl and benzyl bromides, ethyl bromoacetate and ethyl-4-bromocrotonate with 1,2-diones, in the presence of sodium iodide, occur efficiently to afford α-hydroxy keto compounds in excellent yields.

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