3710-30-3 Usage
Description
1,7-Octadiene is a clear, colorless to slightly yellow liquid that is an organic compound with the molecular formula C8H12. It is a diene, which means it contains two carbon-carbon double bonds, and is characterized by its reactivity and potential applications in various chemical processes.
Uses
1. Used in Organic Synthesis:
1,7-Octadiene is used as a building block in organic synthesis for the creation of various complex organic molecules. Its presence of two double bonds allows for a wide range of reactions, making it a versatile compound in the field of organic chemistry.
2. Used in Olefin Ring-Closing Metathesis (RCM) Studies:
1,7-Octadiene is utilized in the study and assessment of the structure and reaction rate in olefin ring-closing metathesis of a series of simple dienes. This process is significant in the synthesis of cyclic compounds, which are essential in the development of pharmaceuticals and other specialty chemicals.
3. Used in Micropatterned Surfaces Research:
1,7-Octadiene has been employed in a study to investigate micropatterned surfaces prepared by plasma polymerization. This research is crucial for the development of advanced materials with specific surface properties, which can be applied in various industries, such as electronics, biotechnology, and nanotechnology.
4. Used as a Crosslinker and Source of Ethylene in Cross-Enyne Metathesis (CEYM)-Related Reactions:
1,7-Octadiene serves as a crosslinker and a source of ethylene for a variant of Mori's conditions in CEYM-related reactions. This application is important in the synthesis of complex organic molecules and polymers, which have a wide range of uses in the chemical, pharmaceutical, and materials science industries.
Flammability and Explosibility
Highlyflammable
Safety Profile
Mildly toxic by ingestion,inhalation and skin contact. A very dangerous fire hazardwhen exposed to heat or flame; can react vigorously withoxidizing materials. When heated to decomposition itemits acrid smoke and irritating fumes.
Check Digit Verification of cas no
The CAS Registry Mumber 3710-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3710-30:
(6*3)+(5*7)+(4*1)+(3*0)+(2*3)+(1*0)=63
63 % 10 = 3
So 3710-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3-4H,1-2,5-8H2
3710-30-3Relevant articles and documents
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Gardner,Wright
, p. 163 (1972)
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Tsuji,J.,Yamakawa,T.
, p. 613 - 616 (1979)
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Takamuku et al.
, p. 2562 (1971)
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Photoredox-Assisted Reductive Cross-Coupling: Mechanistic Insight into Catalytic Aryl-Alkyl Cross-Couplings
Paul, Avishek,Smith, Mark D.,Vannucci, Aaron K.
, p. 1996 - 2003 (2017/02/26)
Here, we describe a photoredox-assisted catalytic system for the direct reductive coupling of two carbon electrophiles. Recent advances have shown that nickel catalysts are active toward the coupling of sp3-carbon electrophiles and that well-controlled, light-driven coupling systems are possible. Our system, composed of a nickel catalyst, an iridium photosensitizer, and an amine electron donor, is capable of coupling halocarbons with high yields. Spectroscopic studies support a mechanism where under visible light irradiation the Ir photosensitizer in conjunction with triethanolamine are capable of reducing a nickel catalyst and activating the catalyst toward cross-coupling of carbon electrophiles. The synthetic methodology developed here operates at low 1 mol % catalyst and photosensitizer loadings. The catalytic system also operates without reaction additives such as inorganic salts or bases. A general and effective sp2-sp3 cross-coupling scheme has been achieved that exhibits tolerance to a wide array of functional groups.