Methyl 3-hydroxypropanoate
Methyl 3-hydroxypropanoate
Resumen del producto
Vista rápida
- Familia de productos
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- Nombre químico
- Methyl 3-hydroxypropanoate
- FM
- C4H8O3
- PM
- 104.10
Methyl 3-hydroxypropanoate is a hydroxy ester identified by CAS 6149-41-3.
This record matches molecular formula C4H8O3, molecular weight about 104.10, PubChem CID 80252, and InChIKey RVGLEPQPVDUSOJ-UHFFFAOYSA-N.
The page uses the verified hydroxy ester identity rather than category-level wording.
Identidad y especificaciones
| Catalog No. | CH56008 |
| CAS No. | 6149-41-3 |
| Chemical Name | Methyl 3-hydroxypropanoate |
| Molecular Formula | C4H8O3 |
| Molecular Weight | 104.10 |
| PubChem CID | 80252 |
| InChIKey | RVGLEPQPVDUSOJ-UHFFFAOYSA-N |
Contexto de aplicación
- Hydroxy ester identity reference: supports matching Methyl 3-hydroxypropanoate with CAS 6149-41-3 and PubChem CID 80252.
- Research intermediate context: useful where a simple hydroxy ester identity must be kept separate from category-level product wording.
- Catalog data alignment: helps compare formula, molecular weight, CAS number, and InChIKey across records.
Información adicional del material
Usos
Useful for aligning Methyl 3-hydroxypropanoate with CAS 6149-41-3, formula C4H8O3, molecular weight about 104.10, PubChem CID 80252, and the InChIKey RVGLEPQPVDUSOJ-UHFFFAOYSA-N.
Características
- Small hydroxy ester identity with formula C4H8O3.
- CAS and exact product-name lookups both resolve to PubChem CID 80252.
- The formula and molecular weight align between CHEMOS source data and PubChem.
Recursos técnicos relacionados
Fuentes públicas
- Propanoic acid, 3-hydroxy-, methyl ester | PubChem CID 80252
- 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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