30315-49-2 Usage
Description
3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is an organic compound characterized by its oxazolidine ring structure and a phenyl group attached to it. It features a 1,1-dimethylethyl group and a hydroxyl group, which contribute to its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is used as an intermediate in the synthesis of pharmaceutical compounds for its ability to form stable and bioactive molecules.
Used in Chemical Synthesis:
3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is used as a building block in the synthesis of various organic compounds, such as 1-Bu amino-3-[(5-phenyl-1,3,4-thiadiazole-2-base) oxygen]-2-propanol maleic acid salt, due to its versatile chemical structure and reactivity.
These applications highlight the potential of 3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol as a valuable compound in the development of new drugs and chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 30315-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,1 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30315-49:
(7*3)+(6*0)+(5*3)+(4*1)+(3*5)+(2*4)+(1*9)=72
72 % 10 = 2
So 30315-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO2/c1-14(2,3)15-9-12(10-16)17-13(15)11-7-5-4-6-8-11/h4-8,12-13,16H,9-10H2,1-3H3
30315-49-2Relevant articles and documents
A Short Chiral Synthesis of 2- and 8-Differently Functionalized 1,4,7,10-TetraoxaspiroUndecane
Lemaire, Marielle,Jeminet, Georges,Dauphin, Gerard
, p. 1907 - 1908 (2007/10/02)
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Certain 1-amino-3-(1-isoquinolinyl)oxy-2-propanol derivatives
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, (2008/06/13)
This invention provides compounds of formula I, STR1wherein R is alkyl of 3 to 7 carbon atoms; cycloalkyl of 3 to 7 carbon atoms; cycloalkyl of 3 to 7 carbon atoms monosubstituted with alkyl of 1 to 4 carbon atoms; α-dialkylpropinyl of 5 to 9 carbon atoms; α-dialkylallyl of 5 to 9 carbon atoms; hydroxyalkyl of 2 to 7 carbon atoms, the hydroxy group thereof being separated by at least two carbon atoms from the nitrogen atom to which R is bound; phenethyl; phenethyl mono- or disubstituted in the phenyl residue independently when di-substituted with halogen of atomic number from 9 to 35, alkyl of 1 to 4 carbon atoms or unbranched alkoxy of 1 to 4 carbon atoms; or adamantyl; and Either R1 is phenyl and R2 is hydrogen; Or R1 is alkyl of 1 to 4 carbon atoms or halogen of atomic number from 9 to 35 and R2 is unbranched alkoxy of 1 to 4 carbon atoms or halogen of atomic number from 9 to 35, with the general proviso that the 8-position of the isoquinoline is unsubstituted and any halogen substituent which may be present in the 3- or 4- position is other than fluorine, Useful for treating coronary diseases, arrhythmia, hyperlipoidemia and hyperglycemia.
