59854-11-4 Usage
Description
TERT-BUTYL 3-HYDROXYPROPIONATE is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds and materials. It is characterized by its functional groups and reactivity, making it a versatile building block in chemical synthesis.
Uses
Used in Pharmaceutical Industry:
TERT-BUTYL 3-HYDROXYPROPIONATE is used as a key starting material for the synthesis of wortmannilactone C, a compound with potential pharmaceutical applications. Its role in the synthesis process is essential for creating the desired end product, which may have therapeutic benefits.
Used in Material Science:
TERT-BUTYL 3-HYDROXYPROPIONATE is used as a precursor to prepare three-dimensional metal-fullerene frameworks (MFFs). These MFFs have unique properties and potential applications in various fields, such as energy storage, catalysis, and electronics. TERT-BUTYL 3-HYDROXYPROPIONATE's ability to form these frameworks highlights its importance in material science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 59854-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59854-11:
(7*5)+(6*9)+(5*8)+(4*5)+(3*4)+(2*1)+(1*1)=164
164 % 10 = 4
So 59854-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O3/c1-7(2,3)10-6(9)4-5-8/h8H,4-5H2,1-3H3
59854-11-4Relevant articles and documents
Stable free radical polymerization - Acrylate alkoxyamine synthesis
Lukkarila, Julie L.,Hamer, Gordon K.,Georges, Michael K.
, p. 5317 - 5319 (2004)
An efficient synthesis of the alkoxyamine containing a benzoyl peroxide fragment, one tert-butyl acrylate monomer unit and TEMPO via an oxymercuration reaction followed by an oxidative demercuration reaction is reported. The formation of significant amounts of an undesired reduced product with the latter reaction was overcome by using a milder reducing agent (NaBH3CN) than those (NaBH4, LiBH4) reported to work well in other systems.