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13119-86-3

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13119-86-3 Usage

Compound Type

Polycyclic aromatic hydrocarbon (PAH) compound

Structure

Five fused benzene rings

Stability

Highly stable

Polarity

Relatively nonpolar

Solubility

Not easily soluble in water

Natural Occurrence

Found in petroleum, coal tar, and various combustion products

Environmental Significance

Used as a marker for environmental pollution caused by fossil fuel combustion

Health Effects

Potential carcinogen and mutagen, associated with respiratory problems and cancer

Monitoring and Reduction Efforts

Efforts are being made to monitor and reduce the presence of 1-methylcoronene in the environment due to its toxic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 13119-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,1 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13119-86:
(7*1)+(6*3)+(5*1)+(4*1)+(3*9)+(2*8)+(1*6)=83
83 % 10 = 3
So 13119-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C25H14/c1-13-12-18-9-8-16-5-3-14-2-4-15-6-7-17-10-11-19(13)25-23(17)21(15)20(14)22(16)24(18)25/h2-12H,1H3

13119-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-METHYLCORONENE

1.2 Other means of identification

Product number -
Other names 1-Methyl-coronen

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:13119-86-3 SDS

13119-86-3Upstream product

13119-86-3Downstream Products

13119-86-3Relevant articles and documents

Short and efficient synthesis of coronene derivatives via ruthenium-catalyzed benzannulation protocol

Shen, Hung-Chin,Tang, Jhih-Meng,Chang, Hsu-Kai,Yang, Chia-Wei,Liu, Rai-Shung

, p. 10113 - 10116 (2007/10/03)

TpRuPPh3(CH3CN)2PF6 (3 mol %) was very active in catalytic benzannulation of 1-phenyl-2-ethynylbenzenes in dichloroethane (60 °C, 36 h) to afford phenanthrene in 95% yield. This method is applicable to the synthesis of various polycyclic aromatic hydrocarbons via two- and four-fold benzannulations, including various substituted coronene derivatives (53-86% yields) using this catalyst at a moderate loading (10 mol %).

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