Hexane-1,6-diol
Hexane-1,6-diol
Résumé du produit
Aperçu rapide
- Famille de produits
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Nom chimique
- Hexane-1,6-diol
- FM
- C6H14O2
- PM
- 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.
Identité et spécifications
| 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 |
Contexte d’application
- 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.
Informations complémentaires sur le matériau
Utilisations
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.
Caractéristiques
- 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.
Ressources techniques associées
Sources publiques
- 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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