Hexane-1,6-diol
Hexane-1,6-diol
Product summary
Quick view
- Product family
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Chemical Name
- Hexane-1,6-diol
- MF
- C6H14O2
- MW
- 118.17
Hexane-1,6-diol is a linear aliphatic diol identified by CAS 629-11-8.
This record matches molecular formula C6H14O2, molecular weight 118.17, PubChem CID 12374, and InChIKey XXMIOPMDWAUFGU-UHFFFAOYSA-N.
The page uses the verified diol identity rather than category-level wording.
Identity and specifications
| Catalog No. | CH56005 |
| CAS No. | 629-11-8 |
| Chemical Name | Hexane-1,6-diol |
| Molecular Formula | C6H14O2 |
| Molecular Weight | 118.17 |
| PubChem CID | 12374 |
| InChIKey | XXMIOPMDWAUFGU-UHFFFAOYSA-N |
Application context
- Diol identity reference: supports matching Hexane-1,6-diol with CAS 629-11-8 and PubChem CID 12374.
- Research intermediate context: useful where a simple linear diol identity must be separated from category-level product wording.
- Catalog data alignment: helps compare formula, molecular weight, CAS number, and InChIKey across records.
Additional material information
Uses
Useful for aligning Hexane-1,6-diol with CAS 629-11-8, formula C6H14O2, molecular weight 118.17, PubChem CID 12374, and the InChIKey XXMIOPMDWAUFGU-UHFFFAOYSA-N.
Characteristics
- Linear six-carbon diol with hydroxyl groups at both terminal positions.
- CAS and exact product-name lookups both resolve to PubChem CID 12374.
- The formula and molecular weight align between CHEMOS source data and PubChem.
Related technical resources
PROTAC / TPD Building Blocks
CRBN and VHL ligand derivatives, ligand-linkers, bifunctional degrader intermediates, and linker-tuning building blocks.
PROTAC Linker Selection
Build linker series from both ligands, exit vectors, ternary-complex geometry, conformation, permeability, synthesis, and assay evidence.
Public references
- 1,6-Hexanediol | PubChem CID 12374
- Catalytic in vivo protein knockdown by small-molecule PROTACs
Nature Chemical Biology, 2015
Product-family technical context
- Structural basis of PROTAC cooperative recognition for selective protein degradation
Nature Chemical Biology, 2017
Product-family technical context
- Structural Basis of PROTAC Cooperative Recognition for Selective Protein Degradation
Nature Chemical Biology, 2017
Product-family technical context
- Direct-to-Biology Accelerates PROTAC Synthesis and the Evaluation of Linker Effects on Permeability and Degradation
ACS Medicinal Chemistry Letters, 2022
Product-family technical context
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