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Spiro[3.4]octan-1-one, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65923-47-9

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65923-47-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65923-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,2 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65923-47:
(7*6)+(6*5)+(5*9)+(4*2)+(3*3)+(2*4)+(1*7)=149
149 % 10 = 9
So 65923-47-9 is a valid CAS Registry Number.

65923-47-9SDS

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 1-phenylspiro[3.4]octan-3-one

1.2 Other means of identification

Product number -
Other names Spiro[3.4]octan-1-one,3-phenyl

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:65923-47-9 SDS

65923-47-9Downstream Products

65923-47-9Relevant academic research and scientific papers

Reactions of Nitrosobenzenes with Cyclobutanones by Activation with a Lewis Acid

Shima, Yusuke,Igarashi, Emiko,Yoshimura, Tomoyuki,Matsuo, Jun-Ichi

, p. 723 - 726 (2018)

Formal [4+2] cycloaddition between 3-ethoxy-2-alkylcyclobutanones and nitrosobenzene proceeded by activation with Me 3 SiOTf to afford 6-alkyl-2-phenyl-2 H -1,2-oxazin-5(6 H)-one by regioselective cleavage of the more substituted C2-C3 bond of the cyclobutanone ring. On the other hand, reactions of 3-phenylcyclobutanones and 2-benzyloxycyclobutanone with nitrosobenzene gave γ,δ-unsaturated and cyclic hydroxamic acid derivatives, respectively, by cleavage of a cyclobutanone C1-C2 bond.

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