147598-21-8 Usage
Description
3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL, also known as 3-[4-(2-Methylpropyl)phenyl]propan-1-ol, is an organic compound with a unique molecular structure that features a propane base with a phenyl group substituted at the 4-position with an isobutyl group. 3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL is characterized by its distinct chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL is used as an intermediate in the chemical synthesis process for the production of various compounds. Its unique structure allows it to be a valuable building block for creating a wide range of molecules with different properties and applications.
Used in Hydrogenation Process:
In the field of chemical engineering, 3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL is used as a reactant in the hydrogenation process. This process involves the addition of hydrogen (H2) to a molecule, typically in the presence of a transition metal complex catalyst with a tridentate or bisdentate ligand. The hydrogenation of 3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL can lead to the formation of new compounds with altered properties, which can be utilized in various applications.
Used in Pharmaceutical Industry:
3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL may also find applications in the pharmaceutical industry, where it can be used as a starting material or intermediate for the synthesis of drugs with potential therapeutic effects. Its unique structure and reactivity make it a promising candidate for the development of new medications.
Used in Flavor and Fragrance Industry:
Due to its distinct chemical properties, 3-(4-ISOBUTYL-PHENYL)-PROPAN-1-OL can be used in the flavor and fragrance industry as a component in the creation of various scents and flavors. Its unique molecular structure can contribute to the development of new and innovative fragrances and taste profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 147598-21-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,9 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147598-21:
(8*1)+(7*4)+(6*7)+(5*5)+(4*9)+(3*8)+(2*2)+(1*1)=168
168 % 10 = 8
So 147598-21-8 is a valid CAS Registry Number.
147598-21-8Relevant articles and documents
IMPROVEMENTS IN OR RELATING TO ORGANIC COMPOUNDS
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Paragraph 0106; 0108; 0109, (2016/11/24)
A process for the hydrogenation of a substrate comprising a carbon heteroatom double bond in the presence of a transition metal complex comprising a tridentate or bisdentate-ligand containing a nitrogen, sulphur and phosphorus atom, of which at least the N- and P- and optionally also the S-atom coordinates with the transition metal.
Accessible protocol for asymmetric hydroformylation of vinylarenes using formaldehyde
Morimoto, Tsumoru,Fujii, Tetsuji,Miyoshi, Kota,Makado, Gouki,Tanimoto, Hiroki,Nishiyama, Yasuhiro,Kakiuchi, Kiyomi
supporting information, p. 4632 - 4636 (2015/04/27)
We report herein on an accessible protocol for the asymmetric hydroformylation of vinylarenes using formaldehyde as a substitute for syngas. The regioselectivity (branched/linear = up to 96/4) and enantioselectivity (up to 95% ee) can be attributed to the use of chiral Ph-bpe as a ligand. This journal is
