76236-32-3 Usage
Description
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one is a chemical compound with the molecular formula C23H23O4. It is a derivative of furan-2(5H)-one, featuring a trityloxy methyl group attached to the 5th position. The trityloxy group serves as a protecting group in organic synthesis, preventing unwanted reactions. (5S)-5-[(trityloxy)methyl]furan-2(5H)-one holds potential applications in organic chemistry, particularly as a building block for synthesizing more complex molecules. Its well-defined structure and properties render it a valuable asset for chemical synthesis and research.
Uses
Used in Organic Chemistry:
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one is used as a building block for the synthesis of complex organic molecules. Its unique structure and the presence of the trityloxy protecting group make it suitable for creating a variety of compounds with specific functionalities and properties.
Used in Chemical Synthesis:
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one is utilized as an intermediate in chemical synthesis processes. The trityloxy group's protective nature allows for selective reactions, enabling the creation of target molecules with greater precision and control over the synthetic pathway.
Used in Research and Development:
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one is employed as a research tool in the field of organic chemistry. Its properties and reactivity can be studied to gain insights into the behavior of similar compounds and to develop new synthetic strategies and methodologies.
Used in Pharmaceutical Industry:
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one may be used as a starting material or intermediate in the development of new pharmaceutical compounds. Its unique structure could potentially be exploited to design novel drugs with specific therapeutic properties.
Used in Material Science:
(5S)-5-[(trityloxy)methyl]furan-2(5H)-one's structural characteristics could also make it a candidate for the development of new materials with specialized properties, such as those with unique optical, electronic, or mechanical characteristics, depending on the final synthesized product.
Check Digit Verification of cas no
The CAS Registry Mumber 76236-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,3 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76236-32:
(7*7)+(6*6)+(5*2)+(4*3)+(3*6)+(2*3)+(1*2)=133
133 % 10 = 3
So 76236-32-3 is a valid CAS Registry Number.
76236-32-3Relevant articles and documents
Synthesis of (+)-muscarine from (S)-(-)-5-hydroxymethyl-2(5H)-furanone
Kyung Ho Kang,Mi Young Cha,Ae Nim Pae,Kyung Il Choi,Yong Seo Cho,Hun Yeong Koh,Bong Young Chung
, p. 8137 - 8140 (2007/10/03)
(+)-Muscarine has been synthesized from (S)-(-)-5-hydroxy-2(5H)-furanone via rather a long pathway to provide easy access to a wide variety of its analogues. (C) 2000 Published by Elsevier Science Ltd.
A synthetic route to 3-C-alkyl (or 3-C-phenyl-) 2,3-dideoxy-D-erythro- pentono-1,4-lactones: Intermediates in the synthesis of 2(3H)-furanones
Raveendranath,Blazis,Agyei-Aye,Hebbler,Gentile,Hawkins,Johnson,Baker
, p. 207 - 223 (2007/10/02)
A series of 3-C-alkyl- (and 3-C-phenyl-) 2,3-dideoxy-D-erythro-pentono- 1,4-lactones, compounds which are important in the synthesis of modified nucleosides and antibiotic sugars, were synthesized from D-ribonolactone. By a route that proceeded via 5-O-pr
A Short Synthesis of (S)-5-Hydroxy-2-penten-4-olide from D-Mannitol via 2,3-O-Isopropylidene-D-glyceraldehyde
Haefele, Brigitte,Jaeger, Volker
, p. 85 - 88 (2007/10/02)
(S)-5-Hydroxy-2-penten-4-olide (5) was synthesized in three steps starting from D-mannitol bis(acetonide) (1), via D-glyceraldehyde acetonide (2) by Z-selective Wittig reaction, acid-catalyzed lactonization and crystallization with a total yield of 40percent.
