162358-04-5 Usage
Description
Benzeneethanol, 4-octyl-1-acetate, also known as 2-(4-Octylphenyl)ethyl Acetate, is an organic compound with the chemical formula C18H26O2. It is an oily liquid with a unique chemical structure that makes it useful in various applications, particularly in organic synthesis.
Uses
Used in Organic Synthesis:
Benzeneethanol, 4-octyl-1-acetate is used as a synthetic building block for the creation of various organic compounds. Its unique chemical structure allows it to be a valuable intermediate in the synthesis of complex molecules, contributing to the development of new materials and chemicals.
Used in Fragrance Industry:
Benzeneethanol, 4-octyl-1-acetate is used as a fragrance ingredient due to its pleasant aroma. It is added to perfumes, colognes, and other scented products to provide a distinct and long-lasting scent.
Used in Flavor Industry:
In addition to its use in the fragrance industry, Benzeneethanol, 4-octyl-1-acetate is also utilized as a flavoring agent in the food and beverage industry. Its unique taste profile adds depth and complexity to various flavors, enhancing the overall sensory experience of the product.
Used in Pharmaceutical Industry:
Benzeneethanol, 4-octyl-1-acetate may also find applications in the pharmaceutical industry, where it can be used as a starting material for the synthesis of various drugs and medicinal compounds. Its versatile chemical structure allows for the development of new therapeutic agents with potential benefits in healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 162358-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,5 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 162358-04:
(8*1)+(7*6)+(6*2)+(5*3)+(4*5)+(3*8)+(2*0)+(1*4)=125
125 % 10 = 5
So 162358-04-5 is a valid CAS Registry Number.
InChI:InChI=1S/C18H28O2/c1-3-4-5-6-7-8-9-17-10-12-18(13-11-17)14-15-20-16(2)19/h10-13H,3-9,14-15H2,1-2H3
162358-04-5Relevant articles and documents
Iron-catalyzed cross-coupling reactions. A scalable synthesis of the immunosuppressive agent FTY720
Seidel, Guenter,Laurich, Daniel,Fuerstner, Alois
, p. 3950 - 3952 (2004)
A chemo- and regioselective cross-coupling reaction of the functionalized aryl triflate 5 with octylmagnesium bromide catalyzed by cheap, nontoxic, and environmentally benign Fe(acac)3 sets the basis for a practical and scaleable synthesis of the octylbenzene derivative 6, which serves as a key building block for the preparation of FTY720 (1). This 2-amino-1,3-propanediol derivative shows highly promising immunosuppressive properties and is currently in human clinical phase III trials.
PREPARATION OF FINGOLIMOD AND ITS SALTS
-
, (2014/09/03)
The present application provide processes for the preparation of fingolimod and its pharmaceutically acceptable salts, process for the purification of fingolimod hydrochloride and process for the preparation of amorphous fingolimod hydrochloride.
Synthesis of selective inhibitors of sphingosine kinase 1
Baek, Dong Jae,MacRitchie, Neil,Pyne, Nigel J.,Pyne, Susan,Bittman, Robert
supporting information, p. 2136 - 2138 (2013/03/28)
Sphingosine kinase isoform 1 (SK1) inhibitors may serve as therapeutic agents for proliferative diseases, including hypertension. We synthesized a series of sphingosine-based SK1-selective inhibitors, the most potent of which is RB-005 (IC50 = 3.6 μM), which also induced proteasomal degradation of SK1 in human pulmonary arterial smooth muscle cells.
