- CAS
- Purity
- 824430-39-9
- 99%
Quality products?make an important contribution to long-term revenue and profitability. Bulk supply high purity 1-Naphthalenecarbonyl chloride, 4-ethyl- 824430-39-9, Paid sample available
Used in Organic Synthesis:
1-Naphthalenecarbonyl chloride, 4-ethylis used as a reagent in organic synthesis for the introduction of the 1-naphthoyl group into other compounds. Its reactivity allows for the formation of various naphthoic acid derivatives, which are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and other organic chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Naphthalenecarbonyl chloride, 4-ethylis used as a key intermediate in the synthesis of various drugs. Its ability to form naphthoic acid derivatives enables the development of new drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
1-Naphthalenecarbonyl chloride, 4-ethylis also utilized in the agrochemical industry for the synthesis of active ingredients in pesticides and other crop protection products. Its introduction of the 1-naphthoyl group into target molecules can enhance the biological activity and selectivity of these agrochemicals.
Used in Dye and Pigment Manufacturing:
In the dye and pigment industry, 1-Naphthalenecarbonyl chloride, 4-ethylis employed in the production of various organic dyes and pigments. Its unique chemical structure contributes to the color properties and stability of these dyes and pigments, making them suitable for use in various applications, such as textiles, plastics, and printing inks.
Used in Production of Other Organic Chemicals:
1-Naphthalenecarbonyl chloride, 4-ethylis also used in the manufacturing of other organic chemicals, such as polymers, surfactants, and fragrances. Its versatility in organic synthesis allows for the development of new chemical entities with diverse applications in various industries.
4-ethyl-1-naphthalenecarboxylic acid
4-ethyl-1-naphthoyl chloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
for 0.25h;
Heating;
|
|
|
With
oxalyl dichloride;
In
dichloromethane;
at 0 ℃;
Reflux;
Inert atmosphere;
|
|
|
With
oxalyl dichloride;
In
N,N-dimethyl-formamide;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
Reflux;
|
|
|
With
oxalyl dichloride;
In
dichloromethane; N,N-dimethyl-formamide;
at 20 ℃;
for 3h;
|
N,N-diphenyl-4-ethyl-1-naphthalenecarboxamide
4-ethyl-1-naphthoyl chloride
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: 90 percent / KOH / bis-(2-hydroxy-ethyl) ether / 8 h / Heating
2: thionyl chloride / 0.25 h / Heating
With
potassium hydroxide; thionyl chloride;
In
diethylene glycol;
|
The CAS number of 1-Naphthalenecarbonyl chloride, 4-ethyl- is 824430-39-9.
More information of 1-Naphthalenecarbonyl chloride, 4-ethyl- 824430-39-9 are:
|
CAS?Number |
824430-39-9 |
|
PSA |
17.07000 |
|
LogP |
3.78120 |
Synonyms?for?1-Naphthalenecarbonyl chloride, 4-ethyl- 824430-39-9:4-ethyl-1-naphthoyl chloride;1-Naphthalenecarbonyl chloride,4-ethyl;
The chemical formula of ?1-Naphthalenecarbonyl chloride, 4-ethyl- is?C13H11ClO which containing 13 Carbon atoms,11 Hydrogen atoms,1 Chlorine atoms and 1 Oxygen atoms,and the molecular weight of??1-Naphthalenecarbonyl chloride, 4-ethyl-?is 218.683.
1-Naphthalenecarbonyl chloride, 4-ethyl-, also known as 4-Ethyl-1-naphthoyl chloride, is a chemical compound with the molecular formula C14H11ClO. It is a derivative of naphthalene, featuring a carbonyl chloride functional group and an ethyl substituent at the 4-position. 1-Naphthalenecarbonyl chloride, 4-ethylis widely used in various applications due to its unique chemical properties and reactivity.
Relevant articles related to 1-Naphthalenecarbonyl chloride, 4-ethyl-:
|
Article |
Source |
|
Enantioselective Arylation of Benzylic C?H Bonds by Copper-Catalyzed Radical Relay |
Zhang, Wen,Wu, Lianqian,Chen, Pinhong,Liu, Guosheng supporting information, p. 6425 - 6429 (2019/04/10) |
|
Synthesis and characterization of cannabimimetic aminoalkylindole based 5-(4-alkyl-1-naphthoylamino)-1,3,4-thiadiazole-2-sulfonamides |
Zengin, Gulay,Nalbantbasi, Zehra,Zengin, Huseyin,Turkmen, Hasan experimental part, p. 707 - 714 (2012/01/05) |
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