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1,2-dimethyl-1,2-dihydroacenaphthylene-1,2-diol is a complex organic compound with the molecular formula C14H14O2. It is a derivative of acenaphthylene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings. The compound is characterized by the presence of two methyl groups (-CH3) attached to the first and second carbon atoms, and two hydroxyl groups (-OH) attached to the same carbon atoms. This structure gives the compound unique chemical and physical properties, making it a potential candidate for various applications in the fields of chemistry and materials science. Due to its complex structure, 1,2-dimethyl-1,2-dihydroacenaphthylene-1,2-diol may exhibit different reactivity and stability compared to its parent compound, acenaphthylene.

6566-38-7

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6566-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6566-38-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6566-38:
(6*6)+(5*5)+(4*6)+(3*6)+(2*3)+(1*8)=117
117 % 10 = 7
So 6566-38-7 is a valid CAS Registry Number.

6566-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R)-1,2-dimethylacenaphthylene-1,2-diol

1.2 Other means of identification

Product number -
Other names cis-1,2-Dimethyl-acenaphthalin-1,2-diol

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

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More Details:6566-38-7 SDS

6566-38-7Relevant academic research and scientific papers

Enantiomerically Enriched α-Borylzinc Reagents by Nickel-Catalyzed Carbozincation of Vinylboronic Esters

Zhang, Chenlong,Hu, Weipeng,Lovinger, Gabriel J.,Jin, Jing,Chen, Jingjia,Morken, James P.

supporting information, p. 14189 - 14195 (2021/09/11)

In this paper is described a synthesis of enantiomerically enriched, configurationally stable organozinc reagents by catalytic enantioselective carbozincation of a vinylboronic ester. This process furnishes enantiomerically enriched α-borylzinc intermediates that are shown to undergo stereospecific reactions, producing enantioenriched secondary boronic ester products. The properties of the intermediate α-borylzinc reagent are probed and the synthetic utility of the products is demonstrated by application to the synthesis of (-)-aphanorphine and (-)-enterolactone.

Diastereoselective and Enantioselective Conjunctive Cross-Coupling Enabled by Boron Ligand Design

Myhill, Jesse A.,Wilhelmsen, Christopher A.,Zhang, Liang,Morken, James P.

supporting information, p. 15181 - 15185 (2018/11/30)

Enantio- and diastereoselective conjunctive cross-coupling of β-substituted alkenylboron "ate" complexes is studied. Whereas β-substitution shifts the chemoselectivity of the catalytic reaction in favor of the Suzuki-Miyaura product, use of a boronic este

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