![1,3,5-Tris(4′-carboxy[1,1′-biphenyl]-4-yl)benzene molecular structure](/images/molecules/1-3-5-tris-4--carboxy-1-1--biphenyl--4-yl-benzene-911818-75-2.png)
Ordering
Available Variants500 mg
CHA.97081-500mg
Price
€105.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.97081-500mg | €105.60 |
95%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C45H30O6 |
|---|---|
| CAS Number | 911818-75-2 |
| Molecular Weight | 666.72 |
| NACRES | NA.23 |
| PubChem Substance ID | 329762673 |
| UNSPSC Code | 26111700 |
| MDL number | MFCD15144773 |
| Assay | 95% |
| Form | powder |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 2 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
Technical Overview & Applications Use-case context
1,3,5-Tris(4′-carboxy[1,1′-biphenyl]-4-yl)benzene, with a CAS number of 911818-75-2, is a complex organic compound that has garnered significant attention in the field of materials science. This molecule exhibits a unique structure, consisting of a central benzene ring substituted with three 4′-carboxy[1,1′-biphenyl]-4-yl groups, which impart its distinctive properties. The presence of carboxylic acid functional groups enables this compound to participate in various chemical reactions, such as esterification and amidation, making it a versatile building block for the synthesis of more complex materials. Furthermore, the biphenyl moieties in this molecule contribute to its potential applications in the development of organic electronic devices, including organic light-emitting diodes and organic photovoltaics, due to their ability to facilitate charge transport and energy transfer.
