Factory Sells Best Quality 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide 81058-27-7 with GMP standards We supply high quality 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide (CAS 81058-27-7), in stock, factory directly supply to clients, lower prices, more competitiveness.
What is the 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide ?
2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide is , while it's Molecular Formula is C26H43BrO9. K?nigs-Knorr glycosyl donor with considerably lower tendency to form orthoester side products during glycosylation than the traditional acetobromoglucose
What is the CAS number for 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide ?
The CAS number of 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide is 81058-27-7.
More information of 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide 81058-27-7 are:
|
Synonyms |
2,3,4,6-Tetra-O-Pivaloyl-α-D-Glucopyranosyl Bromide; |
|
CAS?Number |
81058-27-7 |
|
Molecular Formula |
C26H43BrO9 |
|
Molecular Weight |
579.526 |
|
Density |
1.22g/cm3 |
|
Boiling Point |
530.5oC at 760 mmHg |
|
Flash Point |
274.6oC |
|
HS CODE |
2932990090 |
|
PSA |
114.43000 |
|
LogP |
4.56920 |
What is 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide (81058-27-7) used for?
2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide is a glycosyl donor used in organic synthesis, particularly for the preparation of glycosylated compounds. It is a derivative of alpha-D-glucopyranose, a monosaccharide, with four pivaloyl groups attached to the hydroxyl groups at positions 2, 3, 4, and 6. The bromide group at the anomeric center allows for glycosylation reactions to occur, making it a valuable reagent in carbohydrate chemistry.
InChI:InChI=1/C26H43BrO9/c1-23(2,3)19(28)32-13-14-15(34-20(29)24(4,5)6)16(35-21(30)25(7,8)9)17(18(27)33-14)36-22(31)26(10,11)12/h14-18H,13H2,1-12H3/t14-,15-,16-,17+,18+/m0/s1
Articles related to 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide:
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Article |
Source |
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Excited-State Palladium-Catalyzed 1,2-Spin-Center Shift Enables Selective C-2 Reduction, Deuteration, and Iodination of Carbohydrates |
Zhao, Gaoyuan,Yao, Wang,Mauro, Jaclyn N.,Ngai, Ming-Yu supporting information, p. 1728 - 1734 (2021/02/06) |
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Process for synthesizing card Geleg only (by machine translation) |
- , (2016/12/01) |
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