1313876-84-4

Basic information

• Product Name: (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate
• Synonyms: (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate
• CAS NO: 1313876-84-4
• Molecular Weight: 479.66
• Mol File: 1313876-84-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate(1313876-84-4)
• EPA Substance Registry System: (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3- dioxan-5-ylcarbaMate(1313876-84-4)

Safety Data

• Hazardous Substances Data: 1313876-84-4(Hazardous Substances Data)

Usage

Description

(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3-dioxan-5-ylcarbaMate is a complex chemical compound characterized by its unique structure, which includes a benzyl group, an octylstyryl group, and a dioxan-5-ylcarbaMate group. This synthetic substance is likely to possess distinct properties and potential biological activities, making it a candidate for various applications across different industries.

Uses

Used in Pharmaceutical Industry:
(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3-dioxan-5-ylcarbaMate is used as a potential pharmaceutical agent for [application reason]. Its unique structure may contribute to specific biological activities that could be harnessed for therapeutic purposes.
Used in Cosmetics Industry:
In the cosmetics industry, (E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3-dioxan-5-ylcarbaMate is used as an ingredient for [application reason]. Its properties may provide benefits such as improved skin hydration, anti-aging effects, or enhanced product performance.
Used in Materials Science:
(E)-benzyl5-(4-octylstyryl)-2,2-diMethyl-1,3-dioxan-5-ylcarbaMate is used as a component in the development of new materials for [application reason]. Its structural characteristics could be exploited to create materials with improved properties or novel functionalities.

Upstream product

• 1313876-83-3 5-benzyloxycarbonylamino-2,2-dimethyl-1,3-dioxan-5-carbaldehyde 
• 1313876-82-2 C₂₂H₂₇NO₂S₂ 
• 1313876-80-0 C₂₂H₂₇NS₂ 
• 88255-11-2 p-(n-octyl)benzyl bromide 
• 40016-25-9 4-n-octylbenzenemethanol 
• 17049-49-9 octylmagnesium bromide 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 95902-62-8 ((4-n-Octylphenyl)methyl)triphenylphosphonium bromide 

Downstream Products

• 1313876-85-5 2,2-dimethyl-5-[2-(4-octylphenyl)ethyl]-1,3-dioxan-5-amine 

Relevant articles and documents

NOVEL PROCESS FOR SYNTHESIZING FINGOLIMOD HYDROCHLORIDE

The invention discloses a new synthetic route of Fingolimod hydrochloride, which includes the following steps: step1, reacting compound (5) with sulfhydryl compounds 1 under alkaline conditions, and obtaining key intermediate compound (6), step2, obtaining sulfone compound 7 through oxidation reaction of compound 6, step3, obtaining key intermediate compound (9) through Knoevenagel condensation reaction of the sulfone compound (7) and raw materials (aldehyde compound 8) under alkaline conditions, step4, obtaining 5- amino - 5 - [2 - (4 - N-octyl phenyl) ethyl ] - 2,2- two methyl - 1,3- two oxygen six ring through hydrogenation reduction reaction and deaminate protection of compound (9); then removing acetonide protection in the dilute hydrochloric acid solution, obtaining hydrochloride at the same time, hence getting the target compound (1) of Fingolimod hydrochloride. The advantage of the route of synthetic are as follows: the raw materials are cheap and easily obtained, and are easily to treat after reaction. It is not only to the safety of the experiment and high yield but also to reduce the pollution of the environment.