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Perchlorofulvalene (C14Cl10) is a halogenated hydrocarbon compound consisting of a fulvalene core with ten chlorine atoms attached. Fulvalene is a planar, cyclic hydrocarbon with a structure similar to that of benzene but with an additional carbon atom, forming a seven-membered ring. The perchlorination of fulvalene results in a highly electron-deficient and reactive molecule. Due to its unique structure and properties, perchlorinated fulvalene has potential applications in various fields, such as organic synthesis, materials science, and as a precursor for the synthesis of other complex organic compounds. However, it is important to note that perchlorinated compounds can be hazardous and require proper handling and disposal due to their potential environmental and health risks.

6298-65-3

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6298-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6298-65-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6298-65:
(6*6)+(5*2)+(4*9)+(3*8)+(2*6)+(1*5)=123
123 % 10 = 3
So 6298-65-3 is a valid CAS Registry Number.

6298-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name perchlorofulvalene

1.2 Other means of identification

Product number -
Other names octachloro-bicyclopentadienylidene

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:6298-65-3 SDS

6298-65-3Downstream Products

6298-65-3Relevant academic research and scientific papers

Photochemistry of (η1-C5Cl5)Mn(CO)5 and (η1-C6H5CH2)Mn(CO)5: Competitive formation of 16- and 17e intermediates

Young,Wrighton

, p. 157 - 166 (2007/10/02)

Irradiation of RMn(CO)5 (R = η1-C5Cl5, η1-C6H5CH2) in alkane glasses at 95 K leads to CO loss as the only detectable photoprocess: the ring-slipped (η3-Csu

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