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5,6-dimethylchrysene is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C20H16. It is a derivative of chrysene, a well-known PAH, with two methyl groups attached at the 5th and 6th carbon positions. 5,6-dimethylchrysene is characterized by its complex structure consisting of multiple fused aromatic rings, which contribute to its stability and potential carcinogenic properties. 5,6-dimethylchrysene is formed during the incomplete combustion of organic materials, such as coal, wood, and tobacco, and can be found in various environmental matrices, including air, water, and soil. Due to its potential health risks, it is important to monitor and control the levels of 5,6-dimethylchrysene in the environment and to understand its toxicological effects on humans and other organisms.

3697-27-6

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3697-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3697-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3697-27:
(6*3)+(5*6)+(4*9)+(3*7)+(2*2)+(1*7)=116
116 % 10 = 6
So 3697-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H16/c1-13-14(2)20-17-9-4-3-7-15(17)11-12-19(20)18-10-6-5-8-16(13)18/h3-12H,1-2H3

3697-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethylchrysene

1.2 Other means of identification

Product number -
Other names Chrysene,5,6-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:3697-27-6 SDS

3697-27-6Downstream Products

3697-27-6Relevant academic research and scientific papers

Phenanthrene Synthesis by Palladium(II)-Catalyzed γ-C(sp2)-H Arylation, Cyclization, and Migration Tandem Reaction

Gou, Bo-Bo,Yang, Hui,Sun, Huai-Ri,Chen, Jie,Wu, Junliang,Zhou, Ling

supporting information, p. 80 - 84 (2019/01/11)

Phenanthrene is an important structural motif in chemistry and materials science, and many synthetic routes have been developed to construct its skeleton. However, synthesis of unsymmetric phenanthrenes remains a challenge. Here, an efficient one-pot tandem reaction for the preparation of phenanthrenes via sequential γ-C(sp2)-H arylation, cationic cyclization, dehydration, and 1,2-migration was developed. A wide range of symmetric and unsymmetric phenanthrenes with diversified functional groups were synthesized with good to excellent yields.

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