59697-07-3 Usage
Uses
Used in Organic Synthesis:
(2S-cis)-3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is used as a chiral building block in organic synthesis for the creation of complex organic molecules. Its unique structure allows for the development of enantioselective reactions, which are crucial for producing specific enantiomers of chiral compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, (2S-cis)-3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol serves as a valuable chiral building block for the synthesis of biologically active molecules. Its potential in creating enantiomerically pure compounds makes it an important tool in drug discovery and development.
Used in Organometallic Chemistry:
(2S-cis)-3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is used as a ligand in organometallic chemistry, particularly for the formation of catalysts for asymmetric synthesis. Its ability to form stable complexes with metal centers contributes to the efficiency and selectivity of catalytic processes in various chemical transformations.
Used in Catalyst Development for Asymmetric Synthesis:
In the field of asymmetric synthesis, (2S-cis)-3-(1,1-dimethylethyl)-2-phenyloxazolidine-5-methanol is utilized in the development of catalysts that can selectively produce one enantiomer of a compound over another. This selective synthesis is vital for creating enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 59697-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,9 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59697-07:
(7*5)+(6*9)+(5*6)+(4*9)+(3*7)+(2*0)+(1*7)=183
183 % 10 = 3
So 59697-07-3 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/t12-,13-/m0/s1
59697-07-3Relevant academic research and scientific papers
1-SUBSTITUTED AMINO-3-THIENO-[3,2-c]PYRIDINYLOXY-2-PROPANOLS
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, (2008/06/13)
This invention provides new compounds of formula I, STR1 wherein X is sulphur or oxygen,R is alkyl of 3 to 7 carbon atoms or cycloalkyl of 3 to 7 carbon atoms, cycloalkyl of 3 to 7 carbon atoms monosubstituted by alkyl of 1 to 4 carbon atoms, α-dialkylpropinyl of 5 to 9 carbon atoms or α-dialkyl-allyl of 5 to 9 carbon atoms, hydroxyalkyl of 2 to 7 carbon atoms or phenoxyalkyl of 8 to 11 carbon atoms, the oxygen atom of the last two radicals being separated by at least two carbon atoms from the nitrogen atom to which R is bound, R 1 isI. hydrogen or alkyl of 1 to 4 carbon atoms in the 2,3,6 or 7 position, orIi. chlorine or bromine, in the 2, 3 or 7 position,Iii. nitro or--NHA wherein A is alkanoyl of 1 to 4 carbon atoms, in the 2, 3 or 7 position, orIv. fluorine, cyano or COOB, wherein B is alkyl of 1 to 4 carbon atoms, in the 2 or 3 position, andR 2 isI. hydrogen or alkyl of 1 to 4 carbon atoms in the 2, 3, 6 or 7 position,Ii. chlorine or bromine, in the 2, 3 or 7 position, orIii. fluorine in the 2 or 3 position,Useful in the treatment of heart diseases.
