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4-(Dec-1-yl)-2-oxo-1,3-oxazolidine is a heterocyclic chemical compound characterized by a 1,3-oxazolidine ring with an attached 10-carbon alkyl chain (dec-1-yl group). It has the molecular formula C15H29NO2 and is known for its unique structure and properties that may be beneficial in various applications.

7693-82-5

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7693-82-5 Usage

Uses

Used in Organic Synthesis:
4-(Dec-1-yl)-2-oxo-1,3-oxazolidine is used as a building block or intermediate in organic synthesis for the creation of more complex molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Dec-1-yl)-2-oxo-1,3-oxazolidine is used as a potential active pharmaceutical ingredient (API) or as a key intermediate in the synthesis of APIs. Its heterocyclic nature and the presence of the dec-1-yl group may contribute to the development of new drugs with novel therapeutic properties.
Used in Materials Science:
4-(Dec-1-yl)-2-oxo-1,3-oxazolidine may also find applications in materials science, where its unique structure and properties can be utilized to develop new materials with specific characteristics. This could include the creation of polymers, coatings, or other materials with tailored properties for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7693-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7693-82:
(6*7)+(5*6)+(4*9)+(3*3)+(2*8)+(1*2)=135
135 % 10 = 5
So 7693-82-5 is a valid CAS Registry Number.

7693-82-5Synthetic route

4-methoxy-1,3-oxazolidin-2-one
14441-94-2

4-methoxy-1,3-oxazolidin-2-one

1-bromo dodecane
112-29-8

1-bromo dodecane

4-decyloxazolidin-2-one
7693-82-5

4-decyloxazolidin-2-one

Conditions
ConditionsYield
Stage #1: 1-bromo dodecane With magnesium In tetrahydrofuran at -45℃;
Stage #2: 4-methoxy-1,3-oxazolidin-2-one With copper(I) bromide dimethylsulfide complex; boron trifluoride diethyl etherate In tetrahydrofuran at -50 - 20℃; for 4h; Product distribution / selectivity;
68%
4-methoxy-1,3-oxazolidin-2-one
14441-94-2

4-methoxy-1,3-oxazolidin-2-one

n-decyl magnesium bromide
17049-50-2

n-decyl magnesium bromide

4-decyloxazolidin-2-one
7693-82-5

4-decyloxazolidin-2-one

Conditions
ConditionsYield
With boron trifluoride diethyl etherate; copper(I) cyanide; lithium chloride In tetrahydrofuran at -30℃; Product distribution / selectivity;48%
[1,3]-dioxolan-2-one
96-49-1

[1,3]-dioxolan-2-one

2-amino-1-dodecanol
97028-87-0

2-amino-1-dodecanol

4-decyloxazolidin-2-one
7693-82-5

4-decyloxazolidin-2-one

Conditions
ConditionsYield
In ethyl acetate; toluene27.33 g (96.56%)

7693-82-5Downstream Products

7693-82-5Relevant academic research and scientific papers

Process for the manufacture of alkyl compounds

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Page/Page column 6, (2009/04/23)

Process for the manufacture of a compound of formula I wherein R1 is H, acyl, alkyl or carbamoyl, R2 is a linear alkyl or alkenyl group, preferably a linear alkyl group comprising from 6 to 20 carbon atoms and n is 0, 1, 2, or 3, which comprises reacting a compound of formula II wherein R1 and n are as above and X is a leaving group with a carbanionic reagent of formula II ???????? M-R2 wherein R2 is as above and M denotes a metal or a metal containing group.

Oxazolidinone penetration enhancing compounds

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, (2008/06/13)

Compositions for carrying physiologically active agents through body membranes having the structural formula I: STR1 where: R=H, Alkyl group containing from 1-18 carbon atoms, cycloalkyl, aryl, aralkyl, alkoxy, hydroxyalkyl, alkoyloxyalkyl, acyloxyalkyl and alkoxyalkyl; X=O and NR1, where R1 is selected from H, alkyl, aralkyl acyl group containing from 1-18 carbon atoms, cycloalkyl, hydroxyalkyl, alkoyloxyalkyl acyloxyalkyl and alkoxyalkyl; Y=O and NR2, where R2 is selected from H, alkyl, aralkyl, cycloalkyl, acyl group containing from 1-18 carbon atoms, hydroxyalkyl, alkoyloxyalkyl, acyloxyalkyl and alkoxyalkyl; m=2-4; and n=0-4, are disclosed.

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