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

CAS: 34490-86-3 Cat. No.: D154729 Summenformel: C₁₀H₂₀N₂O₂·2HCl Molekulargewicht: 273.2 EG-Nummer: 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

Übersicht

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

Specifications

Synonyme

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

Spezifikationen & Reinheit

≥98%(T)

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%(T)

Namen und Kennungen

Pubchem Sid

528775753

Kanonisches Lächeln

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

Isomere SMILES

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

WGK Deutschland

3

PubChem CID

118696

Molekulargewicht

273.2

Reaxy-Rn

11334652

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water.
• Empfindlichkeit: Moisture sensitive;Heat sensitive
• Schmelzpunkt (°C): 213-214 °C
• Molekulargewicht: 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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