74801-29-9 Usage
Description
Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is a synthetic compound that is widely used in organic synthesis. It is characterized by its unique structure, which consists of a phenyl group and a tetra-O-benzyl-b-D-thiogalactopyranoside moiety. Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is known for its stability and reactivity, making it a valuable building block in the synthesis of various organic compounds.
Uses
Used in Organic Synthesis:
Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is used as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for the formation of various functional groups and the construction of diverse molecular architectures. Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is used as a building block for the development of new drugs. Its versatility and reactivity enable the synthesis of a wide range of bioactive compounds with potential therapeutic applications. Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside can be used to create novel drug candidates for the treatment of various diseases and disorders.
Used in Agrochemical Industry:
Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is also used in the agrochemical industry for the synthesis of new pesticides and other crop protection agents. Its unique structure allows for the development of innovative molecules with improved efficacy, selectivity, and environmental compatibility.
Used in Specialty Chemicals:
In the specialty chemicals sector, Phenyl2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside is employed in the synthesis of various high-value compounds, such as fragrances, dyes, and functional materials. Its unique properties make it an ideal starting material for the development of novel specialty chemicals with specific applications and performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 74801-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74801-29:
(7*7)+(6*4)+(5*8)+(4*0)+(3*1)+(2*2)+(1*9)=129
129 % 10 = 9
So 74801-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C40H40O5S/c1-6-16-31(17-7-1)26-41-30-36-37(42-27-32-18-8-2-9-19-32)38(43-28-33-20-10-3-11-21-33)39(44-29-34-22-12-4-13-23-34)40(45-36)46-35-24-14-5-15-25-35/h1-25,36-40H,26-30H2/t36?,37-,38?,39?,40-/m0/s1
74801-29-9Relevant articles and documents
First synthesis of bacillus cereus Ch HF-PS cell wall trisaccharide repeating unit
Podilapu, Ananda Rao,Kulkarni, Suvarn S.
, p. 4336 - 4339 (2014)
The first total synthesis of Ch HF-PS, a cell wall trisaccharide repeating unit of B. cereus, is reported. The synthetic trisaccharide is appended with an aminopropyl linker at the reducing end to allow for conjugation to proteins and microarrays. The con
Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of α-Oxo-vinylsulfones to Prepare C-Aryl Glycals and Acyclic Vinyl Ethers
Gong, Liang,Sun, Hong-Bao,Deng, Li-Fan,Zhang, Xia,Liu, Jie,Yang, Shengyong,Niu, Dawen
, (2019/05/22)
We demonstrate that readily available and bench-stable α-oxo-vinylsulfones are competent electrophiles in Ni-catalyzed Suzuki-Miyaura cross-coupling reactions. The C-sulfone bond in the α-oxo-vinylsulfone motif is cleaved chemoselectively in these reactions, furnishing C-aryl glycals or acyclic vinyl ethers in high yields. These reactions proceed under mild conditions and tolerate a remarkable scope of heterocycles and functional groups. Preliminary mechanistic studies revealed the importance of an α-heteroatom in facilitating these transformations.
Visible Light Enables Aerobic Iodine Catalyzed Glycosylation
Krumb, Matthias,Lucas, Tobias,Opatz, Till
, p. 4517 - 4521 (2019/08/06)
A versatile protocol for light induced catalytic activation of thioglycosides using iodine as an inexpensive and readily available photocatalyst was developed. Oxygen serves as a green and cost-efficient terminal oxidant and irradiation is performed with a common household LED-bulb. The scope of this glycosylation protocol was investigated in the synthesis of O-glycosides with yields up to 95 %.