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(2R,4S)-4-isopropyl-2-methoxy-3-((R)-2-methyl-1-(1-methyl-1H-imidazol-2-yl)propyl)oxazolidine is a complex oxazolidine derivative featuring isopropyl, methoxy, and imidazolyl groups. This chiral compound has asymmetric carbon centers at positions 2 and 4, existing as a pair of enantiomers. Its unique structure suggests potential pharmaceutical applications, although further research is required to elucidate its specific properties and uses.

1334170-82-9

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1334170-82-9 Usage

Uses

As the provided materials do not specify any particular applications for (2R,4S)-4-isopropyl-2-methoxy-3-((R)-2-methyl-1-(1-methyl-1H-imidazol-2-yl)propyl)oxazolidine, it is not possible to list its uses based on the information given. However, given its classification as a chemical compound with a complex structure and potential pharmaceutical applications, it can be inferred that (2R,4S)-4-isopropyl-2-methoxy-3-((R)-2-methyl-1-(1-methyl-1H-imidazol-2-yl)propyl)oxazolidine might be used in the development of new drugs or as an intermediate in the synthesis of other bioactive molecules. Further research and experimentation would be necessary to confirm its practical applications and benefits in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1334170-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,1,7 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1334170-82:
(9*1)+(8*3)+(7*3)+(6*4)+(5*1)+(4*7)+(3*0)+(2*8)+(1*2)=129
129 % 10 = 9
So 1334170-82-9 is a valid CAS Registry Number.

1334170-82-9Upstream product

1334170-82-9Downstream Products

1334170-82-9Relevant academic research and scientific papers

Scaffolding catalysts: Highly enantioselective desymmetrization reactions

Sun, Xixi,Worthy, Amanda D.,Tan, Kian L.

, p. 8167 - 8171 (2011)

Ex-changing places: A highly enantioselective desymmetrization of 1,2-diols has been developed in which the catalyst utilizes reversible covalent bonding to the substrate to achieve both high selectivity and rate acceleration (see scheme, PMP=pentalmethyl

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