3-Keto-4-etiocholenic acid methylester

CAS: 2681-55-2

Ref. 3D-FK152624

Produktinformation

• Name: 3-Keto-4-etiocholenic acid methylester
• Synonyme: 4-Androsten-3-one 17β-carboxylic acid methyl ester, Androst-4-Ene-17-Carboxylic Acid, 3-Oxo-, Methyl Ester, (17Beta)-, Androst-4-ene-17-carboxylic acid, 3-oxo-, methyl ester, (17β)-, Androst-4-ene-17β-carboxylic acid, 3-oxo-, methyl ester, L 589.170, Methyl (17beta)-3-oxoandrost-4-ene-17-carboxylate, Methyl (17β)-3-oxoandrost-4-ene-17-carboxylate, Methyl (8Xi,9Xi,14Xi,17Beta)-3-Oxoandrost-4-Ene-17-Carboxylate, Methyl 3-oxo-4-androstene-17.beta.-carboxylate, Methyl 3-oxoandrost-4-ene-17β-carboxylate, Methyl 4-androsten-3-one 17β-carboxylate, Methyl-3-Oxo-4-androstene-17β-carboxylate, Methyl-3-oxo-4-androsten-17β-carboxylate, Methyl-3-oxo-4-androstene-17-carboxylate, Org 7329-0

Beschreibung

3-Keto-4-etiocholenic acid methylester is a chemical that has been shown to have insecticidal properties. 3-Keto-4-etiocholenic acid methylester binds to odorant receptors on the antennae of insects and causes an excitatory response. It can be used as a potential environmental pollutant, as well as an insecticide or repellent. 3-Keto-4-etiocholenic acid methylester binds with high affinity to olfactory receptors in the antennae of insects and has been shown to cause excitation when it comes into contact with these receptors. This compound can be used for screening for new materials with similar odorant binding properties, for research purposes, and also as a biosensor for pollution detection. 3-Keto-4-etiocholenic acid methylester has been shown to react with various substances such as oxygen, nitric oxide, nitrous oxide, sulfur dioxide and

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 330.46 g/mol
• Formel: C₂₁H₃₀O₃
• Reinheit: Min. 95%
• InChl: InChI=1S/C21H30O3/c1-20-10-8-14(22)12-13(20)4-5-15-16-6-7-18(19(23)24-3)21(16,2)11-9-17(15)20/h12,15-18H,4-11H2,1-3H3/t15-,16-,17-,18+,20-,21-/m0/s1
• InChI Key: InChIKey=XWFWMYFLNHTEBF-YFWFAHHUSA-N
• SMILES: COC(=O)[C@H]1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)[C@H]3CC[C@]12C