Welcome to LookChem.com Sign In|Join Free
  • or
Benzenehexacarbonyl hexachloride, also known as C6Cl6(CO)6, is a complex organic compound consisting of a benzene ring with six carbonyl groups (CO) attached to it, each of which is further connected to a chlorine atom. This molecule is characterized by its hexagonal symmetry and the presence of 18 atoms in total, including six carbon atoms from the benzene ring, six carbon atoms from the carbonyl groups, and six chlorine atoms. The compound is of interest in chemical research due to its unique structure and potential applications in the synthesis of other complex organic molecules. It is important to note that the compound is hypothetical and not commonly found in nature or industrial applications, making it a subject of theoretical and academic interest rather than practical use.

4517-27-5

Post Buying Request

4517-27-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4517-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4517-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4517-27:
(6*4)+(5*5)+(4*1)+(3*7)+(2*2)+(1*7)=85
85 % 10 = 5
So 4517-27-5 is a valid CAS Registry Number.

4517-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzene-1,2,3,4,5,6-hexacarbonyl chloride

1.2 Other means of identification

Product number -
Other names Benzolhexacarbonylchlorid

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:4517-27-5 SDS

4517-27-5Upstream product

4517-27-5Relevant academic research and scientific papers

Stacking of a benzenehexacarboxylic acid core in the crystal structure of benzenehexacarboxylic acid α-aminomethyl isobutyrate amide (MA-Aib6)-sodium nitrate complex

Ranganathan,Muraleedharan,Chandrashekhar Rao,Vairamani,Karle,Gilardi

, p. 2544 - 2545 (2001)

MA-Aib6 forms discrete stacks with sandwiched water, sodium and nitrate ions, presenting a novel profile, where nine out of the 12 binding sites, of the six amides present, are involved in bonding with water, sodium and nitrate ions, with no in

N-HALAMINE MELAMINE DERIVATIVES AS NOVEL DECONTAMINATION AND BIOCIDAL AGENTS

-

Paragraph 0084, (2018/04/26)

The present disclosure relates to the field of decontamination and biocidal agents. More specifically, the invention relates to novel N-halamine melamine derivatives, compositions comprising them, processes for their production, and methods using the same

Excited State Luminescence of Multi-(5-phenyl-1, 3, 4-oxadiazo-2-yl) benzenes in an Electron-Donating Matrix: Exciplex or Electroplex?

Yang, Chih-Chiang,Hsu, Chia-Jung,Chou, Pi-Tai,Cheng, Hsu Chun,Su, Yuhlong Oliver,Leung, Man-Kit

experimental part, p. 756 - 768 (2010/06/21)

Multi-(5-phenyl-1, 3, 4-oxadiazo-2-yl)benzenes show emission in organic solvents from ultraviolet to blue (339-447 nm). The reduction potentials E 1/2red cover a large range of -2.11 V for 2, 5-diphenyl-1, 3, 4-oxadiazole to -0.76 V for 1, 2, 3, 4, 5, 6-hexa(5-phenyl-1, 3, 4-oxadiazo-2-yl)benzene. An unexpectedly wide spectral range of the oxadiazole (OXD) exciplex emissions in PVK is observed, ranging from 406 to 603 nm. The OXDs also exhibit similar electroluminescence (EL) when blended into polyvinylcarbazole (PVK). A linear correlation between the λ max of the electroluminescence and photoluminescence is observed, implying that the emission mechanisms in both processes are similar. In addition, the linear correlation between the E1/2red versus λmax of EL (eV) reflected that the term of the charge-transfer configuration of the contact electron-hole pair plays a major role in the exciplex emission. The exciplex EL of 1, 2, 5-tri(5-phenyl-1, 3, 4-oxadiazo-2-yl)benzene (5) could be as high as 1.0 cd/A. Since the exciplex emission usually has a large Stokes shift, this provides a window for us to generate duo emissions for near white light EL with high efficiency. Among the devices we tried, the device of PVK/2-tert-butylphenyl-5-biphenyl-1, 3, 4-oxadiazole/5/2, 5, 8, 11-tetra-tert-butylperylene (100:40:40:4) gave EL with good current efficiency of 1.63 cd/A.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4517-27-5