1000-86-8 Usage
Description
2,4-DIMETHYL-1,3-PENTADIENE is a clear colorless to light yellow liquid that is of interest in the field of chemistry due to its unique structure and properties. It is an organic compound with the molecular formula C7H12 and is characterized by the presence of two methyl groups attached to the second and fourth carbon atoms of a 1,3-pentadiene backbone. 2,4-DIMETHYL-1,3-PENTADIENE has been studied for its various conformational isomers and their vibrational spectra, providing valuable insights into its structure and behavior.
Uses
Used in Chemical Research:
2,4-DIMETHYL-1,3-PENTADIENE is used as a subject of study in chemical research for understanding its conformational isomers and their vibrational spectra. This research helps in gaining insights into the compound's structure, properties, and potential applications in various fields.
Used in Organic Synthesis:
Although not explicitly mentioned in the provided materials, 2,4-DIMETHYL-1,3-PENTADIENE, given its structure and properties, can potentially be used as an intermediate in organic synthesis for the production of various chemicals, pharmaceuticals, and materials. Its reactivity and functional groups make it a candidate for use in the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 1000-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1000-86:
(6*1)+(5*0)+(4*0)+(3*0)+(2*8)+(1*6)=28
28 % 10 = 8
So 1000-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12/c1-6(2)5-7(3)4/h5H,1H2,2-4H3
1000-86-8Relevant articles and documents
Direct episulfidation of alkenes and allenes with elemental sulfur and thiiranes as sulfur sources, catalyzed by molybdenum oxo complexes
Adam, Waldemar,Bargon, Rainer M.,Schenk, Wolfdieter A.
, p. 3871 - 3876 (2003)
The molybdenum oxo complexes 1a and 1b catalyze efficiently the sulfur transfer to a series of alkenes 4 and allenes 6, for which elemental sulfur, phenylthiirane, or methylthiirane have been employed as sulfur sources to afford the corresponding episulfi
Brettle, Cox
, p. 1227 (1969)
Synthesis and X-ray crystal structure of a cationic gold (I) π-(1,3-diene) complex generated via isomerization of a gold π-allene complex
Brown, Timothy J.,Robertson, Bradley D.,Widenhoefer, Ross A.
, p. 25 - 28 (2014)
The cationic gold tetramethylallene complex {[P(t-Bu)2o- biphenyl]Au(η2-Me2CCCMe2)}+ SbF6- (1) underwent formal 1,3-hydrogen migration in CD2Cl2 solution at
Srinivasan,Bone
, p. 550 (1971)
Catalytic hydromagnesation of di- and polymethyl-substituted 1,3-butadienes
Viktorov,Zubritskii
, p. 1755 - 1765 (2007/10/03)
Hydromagnesation of di- and polymethyl-substituted 1,3-butadienes with alkylmagnesium halides in the presence of Ni(PPh3)2Cl2 and NiPy4Cl2 was studied.