Carbofuran-d , CAS No.1007459-98-4

CAS: 1007459-98-4 Cat. No.: C1441063 Summenformel: C₁₂H₁₂D₃NO₃ Molekulargewicht: 224.27 EG-Nummer: 688-570-2 PubChem CID: 16212192

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Übersicht

Carbofuran-d3 is the deuterium labeled Carbofuran.

Specifications

Storage

Store at -20°C

Verschickt in

Ice chest + Ice pads

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

Namen und Kennungen

Kanonisches Lächeln

CC1(CC2=C(O1)C(=CC=C2)OC(=O)NC)C

IUPAC Name

(2,2-dimethyl-3H-1-benzofuran-7-yl) N-(trideuteriomethyl)carbamate

InChIKey

DUEPRVBVGDRKAG-HPRDVNIFSA-N

INCHI

1S/C12H15NO3/c1-12(2)7-8-5-4-6-9(10(8)16-12)15-11(14)13-3/h4-6H,7H2,1-3H3,(H,13,14)/i3D3

Isomere SMILES

[2H]C([2H])([2H])NC(=O)OC1=CC=CC2=C1OC(C2)(C)C

WGK Deutschland

3

PubChem CID

16212192

Molekulargewicht

224.27

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Klasse Coumarans

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Klasse: Coumarans
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Coumarans
• Alternative Parents: Alkyl aryl ethers Benzenoids Carbamate esters Organic carbonic acids and derivatives Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Coumaran - Alkyl aryl ether - Benzenoid - Carbamic acid ester - Carbonic acid derivative - Oxacycle - Ether - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organic oxide - Aromatic heteropolycyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as coumarans. These are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.
• 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