Dimethyl Suberimidate Dihydrochloride - ≥98%(T) , CAS No.34490-86-3

CAS: 34490-86-3 Cat. No.: D154729 Formula: C₁₀H₂₀N₂O₂·2HCl Peso molecolare: 273.2 Numero EC: 252-060-4 PubChem CID: 118696

GRADE & PURITY ≥98%(T)

Synonyms

Dimethyl suberimidate dihydrochloride, 98% | S0246 | SCHEMBL164104 | NSC 163476 | dimethyl octanediimidate 2HCl | Dimethyl suberimidate dihydrochloride, >=98.0% (AT) | 1,8-Dimethoxyoctane-1,8-diyldiammonium dichloride | dimethyl octanebis(imidoate) dihydr

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

Dimethyl suberimidate dihydrochloride acts as a cross-linking agent for amino groups. It is used in the treatment of avian myeloblastosis virus (AMV).

Specifications

Sinonimi

Dimethyl suberimidate dihydrochloride, 98% | S0246 | SCHEMBL164104 | NSC 163476 | dimethyl octanediimidate 2HCl | Dimethyl suberimidate dihydrochloride, >=98.0% (AT) | 1,8-Dimethoxyoctane-1,8-diyldiammonium dichloride | dimethyl octanebis(imidoate) dihydr

Specifiche e purezza

≥98%(T)

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

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

Purezza

≥98%(T)

Nomi e identificatori

Pubchem Sid

528775753

Sorrisi canonici

COC(=N)CCCCCCC(=N)OC.Cl.Cl

IUPAC Name

dimethyl octanediimidate;dihydrochloride

InChIKey

ILKCDNKCNSNFMP-UHFFFAOYSA-N

INCHI

1S/C10H20N2O2.2ClH/c1-13-9(11)7-5-3-4-6-8-10(12)14-2;;/h11-12H,3-8H2,1-2H3;2*1H

Isomeri SMILES

COC(=N)CCCCCCC(=N)OC.Cl.Cl

WGK Germania

3

PubChem CID

118696

Peso molecolare

273.2

Reaxy-Rn

11334652

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboximidic acids and derivatives
      • Subclass Imidoesters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboximidic acids and derivatives
• Subclass: Imidoesters
• Intermediate Tree Nodes: Not available
• Direct Parent: Imidoesters
• Alternative Parents: Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Imido ester - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as imidoesters. These are organic ester derivatives of imidic acid. They have the general structure ROC(CR')=NR\", where R=organyl group, R'-R\"= H or organyl group.
• 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

• Solubilità: Soluble in water.
• Sensibilità: Moisture sensitive;Heat sensitive
• Punto di fusione (°C): 213-214 °C
• Peso molecolare: 273.200 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 9
• Exact Mass: 272.106 Da
• Monoisotopic Mass: 272.106 Da
• Topological Polar Surface Area: 66.200 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 161.000
• 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: 3

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