29097-52-7 Usage
Description
2,2,4,4-Tetramethyl-3-pentanone imine is a unique and stable aliphatic imine, which is a compound containing a carbon-nitrogen double bond. It is characterized by its distinct molecular structure and properties, making it a versatile compound with various applications in different industries.
Uses
Used in Chemical Industry:
2,2,4,4-Tetramethyl-3-pentanone imine is used as a key intermediate in the synthesis of various organic compounds, such as dyes and metabolites. Its stability and unique structure make it a valuable building block for the development of new molecules with potential applications in various fields.
Used in Pharmaceutical Industry:
2,2,4,4-Tetramethyl-3-pentanone imine is used as a starting material for the synthesis of pharmaceutical compounds. Its unique properties allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Dye Industry:
2,2,4,4-Tetramethyl-3-pentanone imine is used as a precursor in the production of dyes. Its stability and reactivity make it an ideal candidate for the development of new dye molecules with improved properties, such as enhanced color intensity and stability.
Synthesis Reference(s)
Journal of the American Chemical Society, 93, p. 4527, 1971 DOI: 10.1021/ja00747a031
Check Digit Verification of cas no
The CAS Registry Mumber 29097-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,0,9 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 29097-52:
(7*2)+(6*9)+(5*0)+(4*9)+(3*7)+(2*5)+(1*2)=137
137 % 10 = 7
So 29097-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H19N/c1-8(2,3)7(10)9(4,5)6/h10H,1-6H3
29097-52-7Relevant articles and documents
Thermal decomposition of O-benzyl ketoximes; role of reverse radical disproportionation
Blake, Jessie A.,Ingold, Keith U.,Lin, Shuqiong,Mulder, Peter,Pratt, Derek A.,Sheeller, Brad,Walton, John C.
, p. 415 - 420 (2007/10/03)
Thermolyses of seven dialkyl, two alkyl-aryl and two diaryl O-benzyl ketoxime ethers, R1R2C=NOCH2Ph, have been examined in three hydrogen donor solvents: tetralin, 9,10-dihydrophenanthrene, and 9,10-dihydroanthracene. All the oxime ethers gave the products expected from homolytic scission of both the O-C bond (viz., R1R2C=NOH and PhCH3) and N-O bond (viz., R1R2C=NH and PhCH2OH). The yields of these products depended on which solvent was used and the rates of decomposition of the O-benzyl oxime ethers were greater in 9,10-dihydrophenanthrene and 9,10-dihydroanthracene than in tetralin. These results indicated that a reverse radical disproportionation reaction in which a hydrogen atom was transferred from the solvent to the oxime ether, followed by β-scission of the resultant aminoalkyl radical, must be important in the latter two solvents. Benzaldehyde was found to be an additional product from thermolyses conducted in tetralin. This, and other evidence, indicated that another induced decomposition mode involving abstraction of a benzylic hydrogen atom, followed by β-scission of the resulting benzyl radical, became important for some substrates. Participation by minor amounts of enamine tautomers of the oxime ethers was shown to be negligible by comparison of thermolysis data for the O-benzyloxime of bicyclo[3.3.1]nonan-9-one, which cannot give an enamine tautomer, with that of the O-benzyloxime of cyclohexanone.
