N-Boc-serinol - ≥97% , CAS No.125414-41-7

CAS: 125414-41-7 Cat. No.: I166730 Peso molecular: 191.22 Número EC: 625-706-1

GRADE & PURITY ≥97%

Synonyms

Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, 1,1-dimethylethyl ester | A890213 | tert-Butyl (1,3-dihydroxypropan-2-yl)carbamate | EN300-84185 | DS-18493 | DTXSID20442706 | SY020146 | tert-butyl 1,3-dihydroxypropan-2-ylcarbamate | N-Boc-serinol, 9

Storage

Room temperature

Shipped In

Normal

Application

227,228,229

Specifications

Sinónimos

Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, 1, 1-dimethylethyl ester | A890213 | tert-Butyl (1, 3-dihydroxypropan-2-yl)carbamate | EN300-84185 | DS-18493 | DTXSID20442706 | SY020146 | tert-butyl 1, 3-dihydroxypropan-2-ylcarbamate | N-Boc-serinol, 9

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 488196751
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488196751
• Sonrisas canónicas: CC(C)(C)OC(=O)NC(CO)CO
• IUPAC Name: tert-butyl N-(1,3-dihydroxypropan-2-yl)carbamate
• InChIKey: JHBKBRLRYPYBLP-UHFFFAOYSA-N
• INCHI: 1S/C8H17NO4/c1-8(2,3)13-7(12)9-6(4-10)5-11/h6,10-11H,4-5H2,1-3H3,(H,9,12)
• Isómeros SMILES: CC(C)(C)OC(=O)NC(CO)CO
• WGK Alemania: 3
• Peso molecular: 191.22
• Reaxy-Rn: 4973554
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4973554&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: Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carbamic acid ester - 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

• Punto de fusión (°C): 85-89℃
• Peso molecular: 191.220 g/mol
• XLogP3: -0.400
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 191.116 Da
• Monoisotopic Mass: 191.116 Da
• Topological Polar Surface Area: 78.800 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 160.000
• 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 Wang, Qinjun Chen, Yifan Luo, Yangqi Qu, Xuwen Li, Haolin Song, Chufeng Li, Yiwen Zhang, Tao Sun, Chen Jiang.  (2024)  Metabolic Nanoregulators Induce Ferroptosis and Change Metabolite Flow to Reverse Immunosuppressive Tumor Microenvironment.  ACS Nano,      [PMID:39666893] [10.1021/acsnano.4c13425]