tert-Butyl 3-(2-Aminoethoxy)propanoate - ≥95% , CAS No.1260092-46-3

CAS: 1260092-46-3 Cat. No.: T405714 Peso molecular: 189.26 Número EC: 878-416-4 PubChem CID: 59256380

GRADE & PURITY ≥95%

Synonyms

SY128689 | MFCD20727480 | SY245056 | tert-butyl 3-(2-aminoethoxy)propanoate | EN300-6493666 | Amino-PEG-t-butyl ester, MW 2,000 | tert-butyl3-(2-aminoethoxy)propanoate | s10504 | 3-(2-aminoethoxy)propionic acid tert-butyl ester | BP-25874 | BP-25875 | 126

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Application

227,228,229

Specifications

Sinónimos

SY128689 | MFCD20727480 | SY245056 | tert-butyl 3-(2-aminoethoxy)propanoate | EN300-6493666 | Amino-PEG-t-butyl ester, MW 2, 000 | tert-butyl3-(2-aminoethoxy)propanoate | s10504 | 3-(2-aminoethoxy)propionic acid tert-butyl ester | BP-25874 | BP-25875 | 126

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504771730
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504771730
• Sonrisas canónicas: CC(C)(C)OC(=O)CCOCCN
• IUPAC Name: tert-butyl 3-(2-aminoethoxy)propanoate
• InChIKey: NSCCYXHEZRMPPH-UHFFFAOYSA-N
• INCHI: 1S/C9H19NO3/c1-9(2,3)13-8(11)4-6-12-7-5-10/h4-7,10H2,1-3H3
• Isómeros SMILES: CC(C)(C)OC(=O)CCOCCN
• PubChem CID: 59256380
• Peso molecular: 189.26
• Reaxy-Rn: 21390248

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid esters
• Alternative Parents: Amino acids and derivatives Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Amino acid or derivatives - Carboxylic acid ester - Dialkyl ether - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Amine - Organic oxygen compound - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carboxylic acid esters. These are carboxylic acid derivatives in which the carbon atom from the carbonyl group is attached to an alkyl or an aryl moiety through an oxygen atom (forming an ester group).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: Light Sensitive,Moisture Sensitive,Heat Sensitive
• Punto de inflamación (°C): 91 °C
• Peso molecular: 189.250 g/mol
• XLogP3: -0.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 189.136 Da
• Monoisotopic Mass: 189.136 Da
• Topological Polar Surface Area: 61.600 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 151.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. ZiYi Wang, SiJia Lin, Xue Dong, Jin Cao, Rong Zhao, Lin Wu, Song Shen.  (2026)  Targeted Degradation of Dipeptidyl Peptidase-4 via Proteolysis-Targeting Chimera Technology for Sustained Glycemic Control in Type 2 Diabetes.  JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:] [10.1021/acs.jmedchem.5c03270]