2-Azidoethanol - ≥95% , CAS No.1517-05-1

CAS: 1517-05-1 Cat. No.: A302966 Molecular Weight: 87.08 EC Number: 808-606-4

GRADE & PURITY ≥95%

Synonyms

Azido-PEG1-alcohol | UNII-D96992S9O1 | HY-138461 | 2-Azido-ethanole, 20 wt% in DCM | 2-Azidoethanole, 20 wt% in toluene | EN300-54800 | CCRIS 4996 | 2-Azidoethanole | LCZC1122 | F8880-1311 | AZIDOETHANOL, 2- | MFCD01940545 | AKOS010631284 | BB 0305512 | 2

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Synonyms

Azido-PEG1-alcohol | UNII-D96992S9O1 | HY-138461 | 2-Azido-ethanole, 20 wt% in DCM | 2-Azidoethanole, 20 wt% in toluene | EN300-54800 | CCRIS 4996 | 2-Azidoethanole | LCZC1122 | F8880-1311 | AZIDOETHANOL, 2- | MFCD01940545 | AKOS010631284 | BB 0305512 | 2

Specifications & Purity

≥95%

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

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

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488187718
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488187718
• Canonical Smiles: C(CO)N=[N+]=[N-]
• IUPAC Name: 2-azidoethanol
• InChIKey: BSULWPSUVMOMAN-UHFFFAOYSA-N
• INCHI: 1S/C2H5N3O/c3-5-4-1-2-6/h6H,1-2H2
• Isomeric SMILES: C(CO)N=[N+]=[N-]
• Molecular Weight: 87.08
• Reaxy-Rn: 1746582
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1746582&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 Alkanolamines Primary alcohols Organopnictogen compounds Organic zwitterions Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Azo imide - Azo compound - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organic zwitterion - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - 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

• Molecular Weight: 87.080 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 87.0433 Da
• Monoisotopic Mass: 87.0433 Da
• Topological Polar Surface Area: 34.600 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 65.200
• 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

References

1. Yibin Yu, Chong Huang, Fen Chen, Weisan Pan, Ling Zhang.  (2022)  Hyaluronan-based theranostic nanomicelles for breast cancer-targeting and anticancer drug delivery.  MATERIALS & DESIGN,      [PMID:] [10.1016/j.matdes.2022.111551]

2. Beibei Lu, Fan Xiao, Zhenyuan Wang, Binshen Wang, Zuchen Pan, Weiwei Zhao, Zhenye Zhu, Jiaheng Zhang.  (2020)  Redox-Sensitive Hyaluronic Acid Polymer Prodrug Nanoparticles for Enhancing Intracellular Drug Self-Delivery and Targeted Cancer Therapy.  ACS Biomaterials Science & Engineering,      [PMID:33463311] [10.1021/acsbiomaterials.0c00762]