4348-68-9 Usage
Description
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA is a chemical compound belonging to the class of organic compounds known as benzoyl glycosides. It is a derivative of alpha-D-arabinofuranose, a naturally occurring sugar molecule, characterized by the presence of three benzoyl groups attached to the arabinofuranose ring. These benzoyl groups serve as protective groups in organic chemistry, preventing unwanted reactions at specific positions in the molecule. The unique structure and reactivity of 2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA make it a promising candidate for various applications in organic synthesis, pharmaceuticals, and medicinal chemistry.
Uses
Used in Organic Synthesis:
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA is used as a key intermediate in the synthesis of various complex organic molecules. Its unique structure and reactivity allow for selective reactions and the formation of diverse chemical products.
Used in Pharmaceutical Industry:
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA is used as a building block for the development of novel pharmaceutical compounds. Its unique structure and reactivity can be exploited to design and synthesize new drugs with improved therapeutic properties.
Used in Medicinal Chemistry:
2 3 5-TRI-O-BENZOYL-ALPHA-D-ARABINO-FURA is used as a versatile tool in medicinal chemistry for the design and optimization of bioactive molecules. Its unique structure and reactivity can be utilized to explore new chemical space and identify potential drug candidates with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 4348-68-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4348-68:
(6*4)+(5*3)+(4*4)+(3*8)+(2*6)+(1*8)=99
99 % 10 = 9
So 4348-68-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H21BrO7/c27-23-22(34-26(30)19-14-8-3-9-15-19)21(33-25(29)18-12-6-2-7-13-18)20(32-23)16-31-24(28)17-10-4-1-5-11-17/h1-15,20-23H,16H2/t20-,21-,22+,23+/m1/s1
4348-68-9Relevant articles and documents
A practical silicon-free strategy for differentiation of hydroxy groups in arabinofuranose derivatives
Abronina, Polina I.,Podvalnyy, Nikita M.,Sedinkin, Sergey L.,Fedina, Ksenia G.,Zinin, Alexander I.,Chizhov, Alexander O.,Torgov, Vladimir I.,Kononov, Leonid O.
experimental part, p. 1219 - 1225 (2012/05/20)
Effective differentiation of 3,5-diol system and 2-hydroxy group in arabinofuranose derivatives, which is required for the preparation of building blocks useful for the synthesis of nucleoside analogues and oligosaccharide fragments of mycobacterial arabinogalactan and lipoarabinomannan, was achieved by using 3,5-di-O-benzoyl-1,2-O-benzylidene-βD-arabinofuranose or 3-O-(chloroacetyl)-β- d-arabinofuranose 1,2,5-orthobenzoate, both readily accessible from inexpensive methylα-d-arabinofuranoside via the corresponding glycosyl bromides. The use of expensive organosilicon protecting groups is completely avoided in this novel strategy, a feature that makes it amenable to scale-up. Georg Thieme Verlag Stuttgart New York.
Ring opening of acylated β-d-arabinofuranose 1,2,5-orthobenzoates with nucleophiles allows access to novel selectively-protected arabinofuranose building blocks
Podvalnyy, Nikita M.,Sedinkin, Sergey L.,Abronina, Polina I.,Zinin, Alexander I.,Fedina, Ksenia G.,Torgov, Vladimir I.,Kononov, Leonid O.
experimental part, p. 7 - 15 (2011/02/26)
β-d-Arabinofuranose 1,2,5-orthobenzoates with 3-O-acetyl, 3-O-benzoyl, and 3-O-chloroacetyl groups were prepared in an efficient manner starting from readily available crystalline methyl 2,3,5-tri-O-benzoyl-α-d- arabinofuranoside, and ring-opening reactio
Conversion of an arabinose-derived allyl vinyl ether system into the functionalized 4-cycloheptenone via Claisen rearrangement
Juers, Stefan,Thiem, Joachim
, p. 843 - 847 (2007/10/03)
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