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2360825-89-2

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2360825-89-2 Usage

Description

(2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid is a complex carboxylic acid derivative featuring a butanoic acid backbone with a fluorenyl side chain, a tert-butoxy group, and a methylamino group. (2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid has a chiral center with an S configuration at the 2nd position and an R configuration at the 3rd position, which may contribute to its unique properties and potential applications in fields such as pharmaceuticals, materials science, and organic chemistry.

Uses

Used in Pharmaceutical Applications:
(2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid is used as a building block for the synthesis of various pharmaceutical compounds due to its unique molecular structure and functional groups. The presence of the fluorenylmethoxy carbonyl group and the chiral center may provide specific biological activities or enhance the compound's pharmacokinetic properties.
Used in Materials Science:
In the field of materials science, (2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid may be utilized as a component in the development of novel materials with tailored properties. (2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid's structural features could be exploited to create materials with specific mechanical, electronic, or optical characteristics.
Used in Organic Chemistry:
(2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid can be employed as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of chemical products. Its unique structure and functional groups make it a valuable starting material for the synthesis of complex organic molecules.
Further research is necessary to fully understand the potential uses and effects of (2S,3R)-3-tert-butoxy-2-[(9H-fluoren-9-ylmethoxy)carbonyl](methyl)aminobutanoic acid in these and other applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2360825-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,3,6,0,8,2 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2360825-89:
(9*2)+(8*3)+(7*6)+(6*0)+(5*8)+(4*2)+(3*5)+(2*8)+(1*9)=172
172 % 10 = 2
So 2360825-89-2 is a valid CAS Registry Number.

2360825-89-2Downstream Products

2360825-89-2Relevant articles and documents

Synthesis of linear undecapeptide precursors of cyclosporin analogues

Galpin,Mohammed,Patel

, p. 1773 - 1782 (2007/10/02)

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