74135-23-2 Usage
Description
Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside, with the CAS number 74135-23-2, is a complex organic compound derived from a sugar molecule. It is characterized by its unique structural features, including the presence of a methyl group, an isopropylidene group, and the absence of a hydroxyl group at the 6th carbon. Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside is primarily utilized in the field of organic synthesis, where it serves as a valuable building block for the creation of more complex molecules.
Uses
Used in Organic Synthesis:
Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside is used as a synthetic intermediate for the development of various complex organic molecules. Its unique structural features make it a versatile compound that can be further modified or functionalized to produce a wide range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside is used as a key component in the synthesis of novel drug candidates. Its unique structure allows for the development of molecules with potential therapeutic applications, such as those targeting specific diseases or conditions.
Used in Chemical Research:
Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside is also used in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic routes. Its unique structural features provide researchers with valuable insights into the reactivity and behavior of similar compounds, ultimately contributing to the advancement of organic chemistry.
Used in Material Science:
In the field of material science, Methyl 6-Deoxy-2-O-methyl-3,4-O-isopropylidene-α-D-galactopyranoside can be used as a building block for the development of new materials with specific properties. Its unique structure may contribute to the creation of materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 74135-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,3 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74135-23:
(7*7)+(6*4)+(5*1)+(4*3)+(3*5)+(2*2)+(1*3)=112
112 % 10 = 2
So 74135-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O5/c1-6-7-8(16-11(2,3)15-7)9(12-4)10(13-5)14-6/h6-10H,1-5H3/t6?,7-,8?,9?,10-/m0/s1
74135-23-2Relevant articles and documents
Iodonium ion-assisted synthesis of tetrameric fragments corresponding to the cell wall phenolic glycolipids of Mycobacterium kansasii serovars II and IV
Zegelaar-Jaarsveld, Korien,Duynstee, Howard I.,Van Der Marel, Gijs A.,Van Boom, Jacques H.
, p. 3575 - 3592 (2007/10/03)
The spacer-containing tetramers 3 and 4, derivatives of the phenolic glycolipids of Mycobacterium kansasii serovars II and IV were prepared by iodonium ion-mediated mannosylation of trimeric acceptor 4-[2-(benzyloxycarbonylamino)ethyl]phenyl 2,4-di-O-methyl-3-O-[4-O-benzyl-2-O-methyl-3-O-(4-O-acetyl-2-O-methyl- α-L-fucopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside (2) with ethyl 1-thio-D-mannopyranoside donors 7, 13 and 24. In addition, the glycosylating properties of donors 7, 13, 24, 29-31, each containing a different protective group at position 2, were examined by executing condensations with model acceptor 18(L) and its enantiomer 18(D).
