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[1,2'-Binaphthalene]-1',4'-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65490-97-3

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65490-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65490-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65490-97:
(7*6)+(6*5)+(5*4)+(4*9)+(3*0)+(2*9)+(1*7)=153
153 % 10 = 3
So 65490-97-3 is a valid CAS Registry Number.

65490-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-1-ylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names [1,2'-Binaphthalene]-1',4'-dione

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:65490-97-3 SDS

65490-97-3Downstream Products

65490-97-3Relevant academic research and scientific papers

Hauser–Kraus Annulation of Phthalides with Nitroalkenes for the Synthesis of Fused and Spiro Heterocycles

Kumar, Tarun,Satam, Nishikant,Namboothiri, Irishi N. N.

, p. 3316 - 3321 (2016/07/26)

Hauser–Kraus annulation of sulfonylphthalides with simple conjugated nitroalkenes follows the expected pathway to furnish naphthoquinones in moderate yields. However, a strategic variation of this reaction by employing nitroalkenes bearing an additional nucleophilic site results in [4+4] annulation leading to complex fused and spiro heterocycles in high yields with high selectivity through a cascade process involving Michael addition, Dieckmann cyclization, and a series of eliminations and rearrangements.

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