N-Boc-diethanolamine - ≥97% , CAS No.103898-11-9

CAS: 103898-11-9 Cat. No.: I165584 Peso molecular: 205.25 Beilstein Registry Number: 4386560 Número EC: 629-288-1

GRADE & PURITY ≥97%

Synonyms

SY018071 | N-Boc-diethanolamine, >=98.0% (GC) | A920565 | Carbamic acid, bis(2-hydroxyethyl)-, 1,1-dimethylethyl ester | tert-Butylbis(2-hydroxyethyl)carbamate | (t-butoxy)-N,N-bis(2-hydroxyethyl)carboxamide | tert-Butyl bis(2-hydroxyethyl)carbamate | t-b

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Application

227,228,229

Specifications

Sinónimos

SY018071 | N-Boc-diethanolamine, >=98.0% (GC) | A920565 | Carbamic acid, bis(2-hydroxyethyl)-, 1, 1-dimethylethyl ester | tert-Butylbis(2-hydroxyethyl)carbamate | (t-butoxy)-N, N-bis(2-hydroxyethyl)carboxamide | tert-Butyl bis(2-hydroxyethyl)carbamate | t-b

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488194835
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488194835
• Sonrisas canónicas: CC(C)(C)OC(=O)N(CCO)CCO
• IUPAC Name: tert-butyl N,N-bis(2-hydroxyethyl)carbamate
• InChIKey: KMUNFRBJXIEULW-UHFFFAOYSA-N
• INCHI: 1S/C9H19NO4/c1-9(2,3)14-8(13)10(4-6-11)5-7-12/h11-12H,4-7H2,1-3H3
• Isómeros SMILES: CC(C)(C)OC(=O)N(CCO)CCO
• WGK Alemania: 3
• Peso molecular: 205.25
• Beilstein: 4386560
• Reaxy-Rn: 4386562
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4386562&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Carbamic acids and derivatives
            • Level7 Carbamate esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Carbamic acids and derivatives
• Direct Parent: Carbamate esters
• Alternative Parents: Alkanolamines Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carbamic acid ester - Alkanolamine - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as carbamate esters. These are compounds containing an ester of carbamic acid with the general structure R2NC(=O)OR' (R' not H). They are esters of carbamic acids.
• 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: Moisture sensitive
• Peso molecular: 205.250 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 6
• Exact Mass: 205.131 Da
• Monoisotopic Mass: 205.131 Da
• Topological Polar Surface Area: 70.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 170.000
• 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. Yu Zou, Quan Zhou, Yinan Zhao, Defu Zhi, Huiying Chen, Rui Wang, Benzhi Ju, Shubiao Zhang.  (2022)  Structure–activity relationships of pH-responsive and ionizable lipids for gene delivery.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:35181463] [10.1016/j.ijpharm.2022.121596]