5340-85-2 Usage
General Description
2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is a chemical compound with the molecular formula C14H22O. It is a clear, colorless liquid with a slightly floral or sweet odor. 2,4-DIMETHYL-4-PHENYLPENTAN-2-OL is commonly used as a fragrance ingredient in perfumes and other scented products. It is also used in the production of various chemical products, such as pharmaceuticals and pesticides. In addition, 2,4-DIMETHYL-4-PHENYLPENTAN-2-OL has been found to exhibit antimicrobial and antioxidant properties, making it potentially useful in a range of applications. However, it is important to handle this chemical with caution, as it can be harmful if ingested or if it comes into contact with the skin or eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 5340-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5340-85:
(6*5)+(5*3)+(4*4)+(3*0)+(2*8)+(1*5)=82
82 % 10 = 2
So 5340-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O/c1-12(2,10-13(3,4)14)11-8-6-5-7-9-11/h5-9,14H,10H2,1-4H3
5340-85-2Relevant articles and documents
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Whitesides,G.M. et al.
, p. 232 - 239 (1972)
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THE EFFECT OF THE POSITION OF THE DOUBLE BOND ON THE MECHANISM OF INTRAMOLECULAR CYCLOALKYLATION OF 2,4-DIMETHYL-4-PHENYLPENTENES IN SULFURIC ACID
Sakhabutdinov, A. G.,Usmanova, A. G.,Frolov, P. A.,Zinchenko, S. V.,Shmidt, F. K.
, p. 1043 - 1047 (2007/10/02)
Hydrogen exchange during the intramolecular cycloalkylation of 2,4-dimethyl-4-phenyylpentenes in 85percent sulfuric acid was studied by NMR and mass spectrometry. It was shown on the basis of the distribution of deuterium in 1,1,3,3-tetramethylindane that during cyclization of the endo-chain olefin the obtained γ-phenylalkyl cation undergoes partial deprotonation with the formation of an isomeric olefin whereas protonation of the terminal double bond is accompanied by rapid alkylation of the aromatic ring.
