4461-48-7 Usage
Description
TRANS-4-METHYL-2-PENTENE is a chemical compound with the molecular formula C6H12. It is a clear, colorless liquid with a faint odor and is classified as an alkene or olefin. It is used in various industrial processes, including as a starting material for the synthesis of other organic compounds and as a solvent in chemical reactions. TRANS-4-METHYL-2-PENTENE is highly flammable and should be handled with care. It is also known to be an irritant to the eyes, skin, and respiratory system and should be used in a well-ventilated area.
Uses
Used in Chemical Synthesis Industry:
TRANS-4-METHYL-2-PENTENE is used as a starting material for the synthesis of other organic compounds, such as pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for various chemical reactions, making it a versatile building block in the synthesis of complex molecules.
Used in Solvent Applications:
TRANS-4-METHYL-2-PENTENE is used as a solvent in chemical reactions, particularly in the production of polymers and resins. Its ability to dissolve a wide range of substances makes it a valuable component in various industrial processes.
Used in Laboratory Research:
TRANS-4-METHYL-2-PENTENE is used in laboratory research for studying chemical reactions and mechanisms, as well as for the development of new synthetic methods and techniques. Its reactivity and stability make it an important tool for chemists in academic and industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 4461-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4461-48:
(6*4)+(5*4)+(4*6)+(3*1)+(2*4)+(1*8)=87
87 % 10 = 7
So 4461-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12/c1-4-5-6(2)3/h4-6H,1-3H3/b5-4+
4461-48-7Relevant articles and documents
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Best,D.C. et al.
, p. 1984 - 1987 (1975)
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Nickel Hydride Complexes Supported by a Pyrrole-Derived Phosphine Ligand
Collett, Joel D.,Guan, Hairong,Krause, Jeanette A.
, p. 345 - 353 (2022/02/16)
The synthesis of two nickel hydride complexes bearing the pyrrole-derived phosphine ligand CyPNH (2-(dicyclohexylphosphino)methyl-1H-pyrrole) was developed, namely, (κP-CyPNH)(κP,κN-CyPN)NiH and the acid-stable trans-(κP-CyPNH)2Ni(OAc)H·HOAc. (κP-CyPNH)(κP,κN-CyPN)NiH stoichiometrically reduces benzaldehyde and acetophenone in a metal-ligand cooperative manner and catalytically dimerizes ethylene and cycloisomerizes 1,5-cyclooctadiene and 1,5-hexadiene. trans-(κP-CyPNH)2Ni(OAc)H·HOAc, available from the protonation of (κP-CyPNH)(κP,κN-CyPN)NiH with acetic acid, catalyzes the cycloisomerization of 1,5-cyclooctadiene more effectively and produces the less thermodynamically favored cycloisomers of 1,5-cyclooctadiene.
METHOD OF PRODUCING TERMINAL DOUBLE BOND-CONTAINING COMPOUND
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Paragraph 0044-0048, (2020/10/09)
SOLUTION: A method of producing a terminal double bond-containing compound includes: reacting a compound represented by the following general formula (I) under a pressure of 0 MPa-G or lower in the presence of a metal oxide catalyst to produce a terminal double bond-containing compound represented by the following general formula (II). In formula (I) and formula (II), R1 and R2 represent hydrocarbon groups, and R1 and R2 may bond each other to form a ring together with carbon atoms by which R1 and R2 bond. EFFECT: According to the present invention, a terminal double bond-containing compound can be safely and easily produced with high selectivity. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT