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Heptaphene, also known as 1,1,2,3,4,5,6-heptachlorocyclohexane, is a synthetic chlorinated hydrocarbon compound that belongs to the group of hexachlorocyclohexane (HCH) isomers. It is a colorless, oily liquid with a chemical formula of C6H7Cl7. Heptaphene is a byproduct of the manufacturing process for the pesticide lindane, which is an isomer of HCH. Due to its toxic properties and potential environmental and health risks, the production and use of heptaphene, along with other HCH isomers, have been restricted or banned in many countries under international agreements such as the Stockholm Convention on Persistent Organic Pollutants.

222-75-3

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222-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222-75-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 222-75:
(5*2)+(4*2)+(3*2)+(2*7)+(1*5)=43
43 % 10 = 3
So 222-75-3 is a valid CAS Registry Number.
InChI:InChI=1/C30H18/c1-3-7-21-13-27-17-29-23(15-25(27)11-19(21)5-1)9-10-24-16-26-12-20-6-2-4-8-22(20)14-28(26)18-30(24)29/h1-18H

222-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name heptaphene

1.2 Other means of identification

Product number -
Other names HEPTAPHENE

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:222-75-3 SDS

222-75-3Downstream Products

222-75-3Relevant academic research and scientific papers

Synthesis of Polycyclic Aromatic Hydrocarbons (PAHs) via a Transient Directing Group

Tang, Ming,Yu, Qinqin,Wang, Ziqi,Zhang, Chen,Sun, Bing,Yi, Ying,Zhang, Fang-Lin

supporting information, p. 7620 - 7623 (2018/12/11)

In this work, an efficient synthetic route was developed to construct PAHs with diverse shape, width, and edge topology. The precursors of PAHs were obtained by using a direct arylation of arenes via a transient ligand-directed C-H functionalization strategy and the cycloaromatization was readily achieved by using a Br?nsted acid catalyst. This novel route provides an opportunity to build up PAHs in a highly efficient manner.

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