GRADE & PURITY ≥97%

Synonyms

3-(2-(2-azidoethoxy)ethoxy)propanoic acid | N3-PEG2-CH2CH2COOH | Azido-PEG2-acid | Azido-PEG2-propionic acid | 9-Azido-4,7-dioxanonanoic acid | HY-140452 | Azido-PEG2-C2-acid | LCZC592 | 1312309-63-9 | ZB0916 | C70430 | 3-[2-(2-azidoethoxy)ethoxy]propanoi

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Application

227,228,229

Specifications

Synonyms

3-(2-(2-azidoethoxy)ethoxy)propanoic acid | N3-PEG2-CH2CH2COOH | Azido-PEG2-acid | Azido-PEG2-propionic acid | 9-Azido-4, 7-dioxanonanoic acid | HY-140452 | Azido-PEG2-C2-acid | LCZC592 | 1312309-63-9 | ZB0916 | C70430 | 3-[2-(2-azidoethoxy)ethoxy]propanoi

Specifications & Purity

≥97%

Biochemical and Physiological Mechanisms

Azido-PEG2-C2-acid is a PEG-based PROTAC linker that is applicable to the synthesis of PROTACs.

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Canonical Smiles: C(COCCOCCN=[N+]=[N-])C(=O)O
• IUPAC Name: 3-[2-(2-azidoethoxy)ethoxy]propanoic acid
• InChIKey: IEHDSRSXQAOLJT-UHFFFAOYSA-N
• INCHI: 1S/C7H13N3O4/c8-10-9-2-4-14-6-5-13-3-1-7(11)12/h1-6H2,(H,11,12)
• Isomeric SMILES: C(COCCOCCN=[N+]=[N-])C(=O)O
• Molecular Weight: 203.20
• Reaxy-Rn: 21362416
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=21362416&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic 1,3-dipolar compounds
    • Class Allyl-type 1,3-dipolar organic compounds
      • Subclass Azo imides

• Kingdom: Organic compounds
• Superclass: Organic 1,3-dipolar compounds
• Class: Allyl-type 1,3-dipolar organic compounds
• Subclass: Azo imides
• Intermediate Tree Nodes: Not available
• Direct Parent: Azo imides
• Alternative Parents: Azo compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Organopnictogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Azo imide - Azo compound - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as azo imides. These are n-Imides of azo compounds, analogous to azoxy compounds, having a delocalized structure.
• 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

Chemical and Physical Properties

• Solubility: Solubility (25°C) In vitro
• Molecular Weight: 203.200 g/mol
• XLogP3: 0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 9
• Exact Mass: 203.091 Da
• Monoisotopic Mass: 203.091 Da
• Topological Polar Surface Area: 70.100 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 203.000
• 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