1210700-52-9 Usage
Uses
Used in Organic Synthesis:
(5-isopropyl-1,3-oxazol-4-yl)methanol(SALTDATA: FREE) is used as a key building block in the field of organic synthesis for the creation of various complex molecules and pharmaceutical compounds. Its unique structure allows for versatile chemical reactions and modifications, contributing to the development of novel molecules with potential applications in different industries.
Used in Drug Discovery:
Used in Research and Development:
(5-isopropyl-1,3-oxazol-4-yl)methanol(SALTDATA: FREE) is also employed in research and development settings, where scientists investigate its properties, behavior, and potential health effects. Understanding these aspects is crucial for ensuring the safe handling and application of the compound in various fields, including pharmaceuticals, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 1210700-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,7,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1210700-52:
(9*1)+(8*2)+(7*1)+(6*0)+(5*7)+(4*0)+(3*0)+(2*5)+(1*2)=79
79 % 10 = 9
So 1210700-52-9 is a valid CAS Registry Number.
1210700-52-9Relevant articles and documents
Expanding the chemical space of sp 3-enriched 4,5-disubstituted oxazoles via synthesis of novel building blocks
Slobodyanyuk, Evgeniy Y.,Andriienko, Andrii A.,Vashchenko, Bohdan V.,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Grygorenko, Oleksandr O.
, p. 421 - 434 (2019)
[Figure not available: see fulltext.] An efficient approach to the preparation of novel sp3-enriched 4,5-disubstituted oxazoles bearing a functional group at the C-4 position is described. The method commenced with synthesis of ethyl oxazole-4-carboxylates (13 examples, 63–99% yield), with subsequent function insertion to the heterocyclic core by late-stage functional group transformation. The LiBH4-mediated reduction of ethyl oxazole-4-carboxylates was the only method which could be optimized at multigram scale (up to 40 g), and its scope was demonstrated by preparation of 13 alcohols with (cyclo)alkyl, fluoroalkyl, or N-Boc-aminoalkyl moiety at the C-5 position (47–89% yield). The utility of these key intermediates was demonstrated by the preparation of chlorides (13 examples, 90–99% yield), azides (13 examples, 83–99% yield), amines (13 examples, 80–98% yield), and sulfonyl chlorides (4 examples, 68–97% yield) – advanced building blocks for synthetic and medicinal chemistry.
