SnAP OA Reagent - ≥95% , CAS No.1577233-70-5

CAS: 1577233-70-5 Cat. No.: S167606 Formula: C₁₆H₃₇NOSn Peso molecolare: 378.18 Numero EC: 809-165-0 PubChem CID: 72734267

GRADE & PURITY ≥95%

Synonyms

1577233-70-5|3-[(Tributylstannyl)methoxy]-1-propanamine|3-((Tributylstannyl)methoxy)propan-1-amine|SnAP OA Reagent|MFCD28579830|3-(tributylstannylmethoxy)propan-1-amine|CNC23370|SY283860|A50108|EN300-305694|[(3-AMINOPROPOXY)METHYL]TRIBUTYLSTANNANE

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinonimi

1577233-70-5 | 3-[(Tributylstannyl)methoxy]-1-propanamine | 3-((Tributylstannyl)methoxy)propan-1-amine | SnAP OA Reagent | MFCD28579830 | 3-(tributylstannylmethoxy)propan-1-amine | CNC23370 | SY283860 | A50108 | EN300-305694 | [(3-AMINOPROPOXY)METHYL]TRIBUTYLSTANNANE

Specifiche e purezza

≥95%

Condizioni di conservazione di stoccaggio

Store at -20°C,Argon charged

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥95%

Nomi e identificatori

• Pubchem Sid: 504772296
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504772296
• Sorrisi canonici: CCCC[Sn](CCCC)(CCCC)COCCCN
• IUPAC Name: 3-(tributylstannylmethoxy)propan-1-amine
• InChIKey: MFLUZZMSFDSMIZ-UHFFFAOYSA-N
• INCHI: 1S/C4H10NO.3C4H9.Sn/c1-6-4-2-3-5;3*1-3-4-2;/h1-5H2;3*1,3-4H2,2H3
• Isomeri SMILES: CCCC[Sn](CCCC)(CCCC)COCCCN
• PubChem CID: 72734267
• Peso molecolare: 378.18

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organo-post-transition metal compounds
      • Subclass Organotin compounds
        • Level5 Tetraorganotin compounds
          • Level6 Tetraalkyltins

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organo-post-transition metal compounds
• Subclass: Organotin compounds
• Intermediate Tree Nodes: Tetraorganotin compounds
• Direct Parent: Tetraalkyltins
• Alternative Parents: Dialkyl ethers Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tetraalkyltin - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as tetraalkyltins. These are tetraorganotin compounds where the tin atom is linked to exactly four alkyl groups.
• 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

Proprietà chimiche e fisiche

• Sensibilità: air & moisture sensitive
• Peso molecolare: 378.200 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 14
• Exact Mass: 379.19 Da
• Monoisotopic Mass: 379.19 Da
• Topological Polar Surface Area: 35.300 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 166.000
• 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

XLogP3

Riferimenti

1. Haichao Li, Deqiang Li, Yuan He, Chaobing Luo, Wu Lan, Arthur J. Ragauskas, Tingting You, Feng Xu.  (2025)  Unleashing the potential of lignin with innovative trifunctional binary deep eutectic solvent strategy: Isolation of uncondensed lignin.  Science Advances,  11  (27):   [PMID:40614203] [10.1126/sciadv.adv7299]