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15,16-Dihydro-3-methylcyclopenta(a)phenanthren-17-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27363-65-1

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27363-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27363-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 27363-65:
(7*2)+(6*7)+(5*3)+(4*6)+(3*3)+(2*6)+(1*5)=121
121 % 10 = 1
So 27363-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O/c1-11-2-4-13-12(10-11)3-5-15-14(13)6-7-17-16(15)8-9-18(17)19/h2-7,10H,8-9H2,1H3

27363-65-1SDS

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 3-methyl-15,16-dihydrocyclopenta[a]phenanthren-17-one

1.2 Other means of identification

Product number -
Other names -

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:27363-65-1 SDS

27363-65-1Downstream Products

27363-65-1Relevant academic research and scientific papers

A Kinetic Investigation of the Hydroxide-catalysed Detritiation of Various -15,16-Dihydrocyclopentaphenanthren-17-ones and Related Compounds

Elvidge, John A.,Jones, John R.,Russell, Jeremy C.,Wiseman, Alan,Coombs, Maurice M.

, p. 563 - 566 (2007/10/02)

The hydroxide-catalysed detritiation rate constants from the C-16 position of a series of substituted -15,16-dihydrocyclopentaphenanthren-17-ones have been measured in a 90:10 (v/v) water-dioxane mixture at 25 deg C.The results show that methyl group substitution brings with it, in addition to the costumary deactivating effect, a marked acceleration in rate, which probably has its origin in steric strain considerations.Similar studies involving the analogous position in a number of related ketones (benzindanone, indanone, and cyclopentanone) show that the rates are not simply a function of the number of additional benzene rings but depend on their position relative to the cyclopentanone system.

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