14333-95-0

Basic information

• Product Name: Benzeneacetaldehyde, a-oxo-4-pentyl-
• CAS NO: 14333-95-0
• Molecular Formula: C13H16O2
• Molecular Weight: 204.269
• Mol File: 14333-95-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzeneacetaldehyde, a-oxo-4-pentyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetaldehyde, a-oxo-4-pentyl-(14333-95-0)
• EPA Substance Registry System: Benzeneacetaldehyde, a-oxo-4-pentyl-(14333-95-0)

Safety Data

• Hazardous Substances Data: 14333-95-0(Hazardous Substances Data)

Upstream product

• 64328-68-3 2-bromo-1-(4-pentylphenyl)ethan-1-one 
• 538-68-1 pentylbenzene 
• 138913-07-2 4-n-pentylbenzamide 
• 10270-29-8 p-n-pentylbenzonitrile 
• 49763-65-7 4-pentylbenzoyl chloride 
• 26311-45-5 4-pentylbenzoic acid 
• 37593-02-5 4-n-pentylacetophenone 

Downstream Products

• 1092390-04-9 4-(4-pentylphenyl)-1,3-dihydroimidazole-2-thione 
• 1092390-05-0 1-hydroxy-4-(4-pentylphenyl)-1,3-dihydroimidazole-2-thione 
• 1092390-06-1 1-hydroxy-5-(4-pentylphenyl)-1,3-dihydroimidazole-2-thione 
• 94775-70-9 2-Hydroxy-1-(4-pentyl-phenyl)-heptane-1,4-dione 
• 94775-80-1 3-(4-Pentyl-phenyl)-6-propyl-pyridazine 
• 94775-61-8 Potassium; 2-[1-hydroxy-2-oxo-2-(4-pentyl-phenyl)-ethyl]-3-oxo-hexanoate 

Relevant articles and documents

One-pot three-component reactions of methyl ketones, phenols and a nucleophile: An expedient way to synthesize densely substituted benzofurans

Three-component reactions of phenylglyoxal monohydrate, phenols, and indoles were developed with the aid of acid-catalyst, which produced various densely substituted benzofurans with good to excellent yields. On the basis of this observation, a one-pot, step-wise reaction was developed by using methyl ketones instead of using phenylglyoxal component in I2/DMSO system. At last, three-component reaction offered a useful way to synthesize densely substituted benzofurans starting from simple and easily available substrates. The indole component can be replaced by some other nucleophiles, such as 1,2,4-trimethoxybenzene and thiophenol.

3-ALKYLIDENEHYDRAZINO SUBSTITUTED HETEROARYL COMPOUNDS AS THROMBOPOIETIN RECEPTOR ACTIVATORS

A compound represented by the formula (1): wherein A is a nitrogen atom or CR4, B is an oxygen atom, a sulfur atom or NR9 (provided that when A is a nitrogen atom, B is not NH), R1 is a C2-14; aryl group, L1 is a bond, CR10R11, an oxygen atom, a sulfur atom or NR12, X is OR13, SR13 or NR14NR15, R2 is a hydrogen atom, a formyl group, a C1-10; alkyl group or the like, L2 is a bond or the like, L3 is a bond, CR17R18, an oxygen atom, a sulfur atom or NR19, L4 is a bond, CR20R21, an oxygen atom, a sulfur atom or NR22, Y is an oxygen atom, a sulfur atom or NR23, and R3 is a C2-14; aryl group, a tautomer, prodrug or pharmaceutically acceptable salt of the compound or a solvate thereof.

Synthesis and Liquid Crystalline Phases of Pyridazine Derivatives II

Four more pyridazine compounds were synthesized.The compounds have a general structure R-X-Y-Z-R'; where Y is 3,6 disubstituted pyridazine ring, X and Z are either trans cyclohexyl or phenyl rings, R and R' are n-alkyl groups.The structure assignments were confirmed by carbon 13 NMR.Their liquid crystalline properties were evaluated.When both X and Z are cyclohexyl rings, the compounds have a single smectic b phase.However, if a phenyl ring is introduced into the system, the morphology becomes complicated.Keywords: synthesis, pyridazine, smectic, classification