![[Bis(trifluoroacetoxy)iodo]benzene 97%](/deepweb/assets/sigmaaldrich/product/structures/238/293/71fcde9a-4afb-4cf5-9c22-8d8d68bf1ba4/640/71fcde9a-4afb-4cf5-9c22-8d8d68bf1ba4.png)
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$52.15
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1 G
$52.15
About This Item
Linear Formula:
C6(C6H5)6
CAS Number:
Molecular Weight:
534.69
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
$52.15
List Price$54.90Save 5%Web-Only Promotion
Available to ship onApril 22, 2025Details
Request a Bulk Order
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Quality Level
assay
98%
form
solid
mp
>300 °C (lit.)
functional group
phenyl
SMILES string
c1ccc(cc1)-c2c(-c3ccccc3)c(-c4ccccc4)c(-c5ccccc5)c(-c6ccccc6)c2-c7ccccc7
InChI
1S/C42H30/c1-7-19-31(20-8-1)37-38(32-21-9-2-10-22-32)40(34-25-13-4-14-26-34)42(36-29-17-6-18-30-36)41(35-27-15-5-16-28-35)39(37)33-23-11-3-12-24-33/h1-30H
InChI key
QBHWPVJPWQGYDS-UHFFFAOYSA-N
Related Categories
application
Hexaphenylbenzene can be used as a starting material to synthesize:
- 1,2,3,4,5,6-Hexacyclohexylcyclohexane by Pd/C catalyzed hydrogenation reaction.[1]
- Stable hexatrityl cations[2] and porous organic polymers[3] for applications in catalysis and gas storage.
- Hexa-peri-hexabenzocoronene via one-pot substitution and oxidative cyclodehydrogenation reaction in the presence of t-BuCl/FeCl3.[4]
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Vandana Bhalla et al.
Chemical communications (Cambridge, England), 49(9), 895-897 (2012-12-19)
Fluorescent nanorods formed by self-assembly of hexaphenylbenzene derivative in the presence of cyanide ions serve as a sensitive colorimetric and fluorogenic sensor for the detection of trinitrotoluene (TNT) at the attogram (10(-18) g) level with a detection limit of 10.21
Synthesis and isolation of polytrityl cations by utilizing hexaphenylbenzene and tetraphenylmethane scaffolds
Rathore R, et al.
The Journal of Organic Chemistry, 69(5), 1524-1530 (2004)
Porous organic polymers based on propeller-like hexaphenylbenzene building units
Chen Q, et al.
Macromolecules, 44(14), 5573-5577 (2011)
From Hexaphenylbenzene to 1,2,3,4,5,6-Hexacyclohexylcyclohexane
Dillenburger M, et al.
Journal of the American Chemical Society, 142(30), 12916-12920 (2020)
A Practical One-Pot Synthesis of Soluble Hexa-peri-hexabenzocoronene and Isolation of Its Cation-Radical Salt
Rathore R and Burns CL
J. Org. React., 68(10), 4071-4074 (2003)
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