fenoxycarb

Synonyms: "insegar", "varikill", "fenasulam", "pictyl", "pyctyl", "ethyl (2-(4-phenoxyphenoxy)ethyl)carbamate", "N-(2-(p-phenoxyphenoxy)ethyl)carbamic acid", "(2-(4-phenoxyphenoxy)ethyl)carbamic acid ethyl ester"

Source: fenoxycarb is a carbamate insect growth regulator.

Identifiers:

IUPAC Name: ethyl N-[2-(4-phenoxyphenoxy)ethyl]carbamate
CAS Number: 72490-01-8 (formerly 79127-80-3)
PubChem ID: 51605
InChiKey: HJUFTIJOISQSKQ-UHFFFAOYSA-N
Canonical SMILES: CCOC(=O)NCCOC1=CC=C(C=C1)OC2=CC=CC=C2

Structural Properties:

Molecular Formula: C17H19NO4
Molecular Weight: 301.337

Pharmacophore Features:

Number of bond donors: 1
Number of bond acceptors: 2
Number of atoms different from hydrogen: 22

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors
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Schmuck G, Mihail F. 2004. Effects of the carbamates fenoxycarb, propamocarb and propoxur on energy supply, glucose utilization and SH-groups in neurons. Arch Toxicol 78(6):330-337.

Smulders CJ, Bueters TJ, Van Kleef RG, Vijverberg HP. 2003. Selective effects of carbamate pesticides on rat neuronal nicotinic acetylcholine receptors and rat brain acetylcholinesterase. Toxicol Appl Pharmacol 193(2):139-146.

Tatarazako N, Oda S, Watanabe H, Morita M, Iguchi T. 2003. Juvenile hormone agonists affect the occurrence of male Daphnia. Chemosphere 53(8):827-833.

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