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9,10-DIMETHYLPHENANTHRENE is a polycyclic aromatic hydrocarbon (PAH) compound characterized by three fused benzene rings with two methyl groups at the 9th and 10th carbon positions. It is a colorless to light yellow solid with a molecular weight of 226.32 g/mol. 9,10-DIMETHYLPHENANTHRENE is mainly utilized as a research chemical and is not extensively applied in commercial settings. Its potential applications in organic synthesis, chemical reactions, and as a building block for novel organic compounds make it a subject of interest for scientists and researchers. Additionally, it may have implications in materials science and pharmaceutical research. However, due to its potential health and environmental hazards, careful handling and storage are required.

604-83-1

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604-83-1 Usage

Uses

Used in Research Chemicals:
9,10-DIMETHYLPHENANTHRENE is used as a research chemical for its potential applications in organic synthesis and chemical reactions. It serves as a building block in the production of novel organic compounds, contributing to the advancement of scientific knowledge in these fields.
Used in Organic Synthesis:
In the field of organic synthesis, 9,10-DIMETHYLPHENANTHRENE is used as a precursor or intermediate in the synthesis of various organic compounds. Its unique structure allows for the development of new chemical pathways and the creation of innovative molecules with potential applications in various industries.
Used in Chemical Reactions:
9,10-DIMETHYLPHENANTHRENE is employed in chemical reactions to study its reactivity and to explore its potential as a catalyst or reactant in various processes. This helps researchers understand its properties and behavior under different conditions, which can lead to the discovery of new chemical reactions and processes.
Used in Materials Science:
In materials science, 9,10-DIMETHYLPHENANTHRENE may have potential applications due to its unique structure and properties. Researchers are interested in exploring its use in the development of new materials with specific characteristics, such as improved stability, conductivity, or other desirable properties.
Used in Pharmaceutical Research:
9,10-DIMETHYLPHENANTHRENE may also have potential applications in the field of pharmaceutical research. Its unique structure could be utilized in the development of new drugs or drug delivery systems, contributing to advancements in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 604-83-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 604-83:
(5*6)+(4*0)+(3*4)+(2*8)+(1*3)=61
61 % 10 = 1
So 604-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H14/c1-11-12(2)14-8-4-6-10-16(14)15-9-5-3-7-13(11)15/h3-10H,1-2H3

604-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,10-DIMETHYLPHENANTHRENE

1.2 Other means of identification

Product number -
Other names Phenanthrene, 9,10-dimethyl-

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:604-83-1 SDS

604-83-1Relevant academic research and scientific papers

Palladium-catalyzed site-selective C(sp3)-H arylation of phenylacetaldehydes

Gou, Bo-Bo,Liu, Hang-Fan,Chen, Jie,Zhou, Ling

supporting information, p. 7084 - 7088 (2019/09/30)

We describe a Pd-catalyzed selective C-H arylation reaction of phenylacetaldehydes using l-valine as the transient directing group. This process showed a broad substrate scope and excellent selectivity in which a ligand-controlled functionalization of the

Flow-vacuum pyrolysis of 2,5-diphenyl-4-methyloxazole

Banciu, Mircea D.,Istrati, Daniela,Schiketanz, Iosif,Mihǎiescu, Dan,Drǎghici, Constantin,Malacea, Raluca

, p. 493 - 499 (2007/10/03)

The flow-vacuum pyrolysis of 2,5-diphenyl-4-methyloxazole (4) at 1000°C and 0.5 Torr afforded a complex reaction mixture containing: benzonitrile, diphenylmethane, 9,10-dimethylphenantrene, 9,10-dimethylantracene, fluorene, o-benzylbenzonitrile (major product, 20-22%), phenanthrene, anthracene, o,o′-dicyanodiphenyl, 9,10-anthraquinone, 2-methyl-4,5-diphenyloxazole and 1,1,2,2-tetraphenylethane. A radical- and carbene mechanism is suggested in order to rationalize the formation of the reaction products.

Dramatic influence of nitrogen heterocycles on the activity of low-valent titanium reagent: An improved one-pot synthesis of phenanthrenes

Kadam,Nayak,Banerji

, p. 135 - 142 (2007/10/02)

A novel low-valent titanium (LVT) induced one-pot synthesis of phenanthrenes (25-38% yield) from ortho-alkoxy aromatic aldehydes/ketones was reported by us earlier. Activity of LVT complex could be modulated rationally by using catalytic amount of pyridine. Use of this LVT-pyridine reagent system improved the yields of phenanthrenes (3) by two folds.

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