4,6,8-trimethylazulene is a member of the class of azulenes that is azulene substituted by methyl groups at positions 4, 6 and 8 respectively. It has a role as a metabolite. It derives from a hydride of an azulene.


1-Acetyl-4,6,8-trimethylazulene | C15H16O | CID 607590 - structure, chemical names, physical and chemical properties, classification, patents, literature, 

Formula: C 13 H 14; Molecular weight: 170.2503; IUPAC Standard InChI: 4,6,8-TRIMETHYLAZULENE Aldrich CPR. CAS Number 941-81-1. Linear Formula C 13 H 14. Molecular Weight 170.257 . MDL number MFCD00042693 Molecular Formula: C 13 H 14.

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Molecular Formula: C 13 H 14. Molecular Weight: 170.254 g/mol. Cas Number: 941-81-1. EINECS Number: n/a. MDL Number: MFCD00042693. InChIKey: RUNBRXWUHPOTOO-UHFFFAOYAT. Smiles: …

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Acylated trimethylazulene

Angew. Chem. Int. Ed. First fatty acylated dipeptides to affect muscarinic receptor ligand binding. Bioorg. Med. 4 Feb 2021 This was followed by the six-step synthesis of azulene from naphthalene The colourful chemistry in Loughborough, with its synthesis of acyl  acylation of nucleophilic residues found in the active sites of en- zymes by the azulene skeleton, with chlorosufonyl isocyanate delivered spiro-b- lactam 31 in  Calixazulenes: azulene-based calixarene analogues - an overview and recent Modification and Unexpected Reactivity of 2-Borylbenzaldimines: Acylated and  22, Azulene furan, C15H10O2, 222, 23.867, 0.58 or C-11 of compounds were mainly substituted by acyl groups such as acetyl, isovaleryl, α-acetoxyisovaleryl,   novel route to azulene itself from 6-dimethylaminofulvene by the action of acetic anhydride on N-acyl- preparation of a more stable formylated or acylated . 1 Sep 1992 reaction fails, whereas nucleophilic aromatic compounds like azulene, phenol,. N ,N-dimethylaniline and indole all give the expected products  15 May 2013 3.1 Azulene Formation Selective substitutions of the acyl groups of thapsigargin.

Acylated trimethylazulene

Predicted data is generated using the US Environmental Protection Agency’s EPISuite™. Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = 4.30 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 312.70 (Adapted Stein & Brown method) Melting Pt (deg C): 94.21 (Mean or Weighted MP) VP(mm Hg,25 deg C): 0.000402 (Modified Grain method 4,6,8-trimethylazulene - cas 941-81-1, synthesis, structure, density, melting point, boiling point 4,6,8-Trimethylazulene with trifluoroacetic anhydride Product is acylated trimethylazulene. Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is reaction small amounts of acylated benzoic acid 6a or phthalide 4a were obtained. Therefor e, this reaction . as 4,6,8-trimethylazulene, was . The acylated amines 4 and 5 were hydrolyzed in almost quantitative yields to Starting from amine 6b and guaiazulene/starting from amine 6c and 4,6,8-trimethylazulene. With certain of the 1-trichloroacetyl compounds, reaction with base resulted in the loss or transformation of the acyl group rather then cyclization.
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Acylated trimethylazulene

e. Molecular Formula C. 15.

Dipeptide synthesis from N-[3-(2-furyl)acryloyl]-acylated (Fua-) amino acid ethyl ester and amino acid amide catalyzed by wheat bran carboxypeptidase (carboxypeptidase W) was studied.
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This enzyme belongs to the family of lyases, specifically the aldehyde-lyases, which cleave carbon-carbon bonds. This enzyme participates in methane metabolism.

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