55707-41-0 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1,1-DiMethoxy-2-propanaMine is used as a synthetic intermediate for the development of N-protected α-amino aldehydes, which are crucial components in the synthesis of peptide aldehydes with enzyme inhibitor activity. One such example is Leupeptin, a potent and widely used inhibitor of various proteases, including trypsin, chymotrypsin, and thrombin. These enzyme inhibitors play a significant role in the research and treatment of various diseases, including cancer and inflammatory conditions.
Used in Chemical Industry:
(S)-1,1-DiMethoxy-2-propanaMine is also used as a building block for the preparation of amino sugars and unusual amino acids. Amino sugars are essential components of various biological molecules, such as glycoproteins and glycolipids, which are involved in numerous cellular processes, including cell signaling, adhesion, and immune response. Unusual amino acids, on the other hand, are used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 55707-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55707-41:
(7*5)+(6*5)+(5*7)+(4*0)+(3*7)+(2*4)+(1*1)=130
130 % 10 = 0
So 55707-41-0 is a valid CAS Registry Number.
55707-41-0Relevant academic research and scientific papers
Protecting-group-free total synthesis of (-)-rhazinilam and (-)-rhazinicine using a gold-catalyzed cascade cyclization
Sugimoto, Kenji,Toyoshima, Kazuki,Nonaka, Shiori,Kotaki, Kenta,Ueda, Hirofumi,Tokuyama, Hidetoshi
supporting information, p. 7168 - 7171 (2013/07/26)
'Rhaz'zmatazz: A total synthesis of (-)-rhazinilam and the first asymmetric total synthesis of (-)-rhazinicine were accomplished by using constructing the indolizinone core through the gold-catalyzed cyclization of a fully elaborated linear ynamide. The scope and generality of this cascade reaction for the construction of highly substituted indolizinones were also investigated. Copyright
Solid-phase synthesis of C-terminal peptide aldehydes from amino acetals anchored to a backbone amide linker (BAL) handle
Guillaumie,Kappel,Kelly,Barany,Jensen
, p. 6131 - 6135 (2007/10/03)
Peptide aldehydes were synthesized, starting from amino acetals, by a Solid-phase backbone amide linker (BAL) strategy. (C) 2000 Elsevier Science Ltd.
A Simple, Chiral-Pool-Independent Synthesis of Enantiomerically Pure Alanine-Derived α-Amino Aldehyde Acetals
Bringmann, Gerhard,Geisler, Joerg-Peter
, p. 608 - 610 (2007/10/02)
Enantiomerically pure (R)- or (S)-1,1-dialkoxy-2-propanamines 5 are obtained in good chemical and optical yields, by asymmetric reduction of chiral imines prepared from 1,1-dialkoxy-2-propanones, using (R)- or (S)-1-phenylethylamine ((R)- or (S)-2) as an
