428816-48-2 Usage
Uses
Used in Organic Chemistry:
2,3,4,6-TETRA-O-BENZOYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE is used as a reagent for the protection of hydroxyl groups in carbohydrate synthesis, enabling the formation of various glycosidic linkages for the production of complex carbohydrate structures.
Used in Pharmaceutical Development:
2,3,4,6-TETRA-O-BENZOYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE is used as a building block in the development of pharmaceuticals and other bioactive molecules, due to its unique chemical properties and structural features that contribute to the creation of novel therapeutic agents.
Used in the Formation of Amides and Related Compounds:
2,3,4,6-TETRA-O-BENZOYL-ALPHA-D-GLUCOPYRANOSYL P-TRIFLUOROMETHYLBENZYLTHIO-N-(P-TRIFLUOROMETHYLPHENYL)FORMIMIDATE is used as a formimidate in the synthesis of amides and other related compounds, providing a versatile approach to the creation of diverse chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 428816-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,8,8,1 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 428816-48:
(8*4)+(7*2)+(6*8)+(5*8)+(4*1)+(3*6)+(2*4)+(1*8)=172
172 % 10 = 2
So 428816-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C50H37F6NO10S/c51-49(52,53)36-23-21-31(22-24-36)30-68-48(57-38-27-25-37(26-28-38)50(54,55)56)67-47-42(66-46(61)35-19-11-4-12-20-35)41(65-45(60)34-17-9-3-10-18-34)40(64-44(59)33-15-7-2-8-16-33)39(63-47)29-62-43(58)32-13-5-1-6-14-32/h1-28,39-42,47H,29-30H2/b57-48-/t39-,40-,41+,42-,47-/m1/s1
428816-48-2Relevant academic research and scientific papers
Catalytic and stereoselective glycosylation with a novel and efficient disarmed glycosyl donor: Glycosyl p-trifluoromethylbenzylthio-p-trifluoromethylphenyl formimidate
Mukaiyama, Teruaki,Chiba, Hiroyuki,Funasaka, Setsuo
, p. 392 - 393 (2007/10/03)
A novel and efficient glycosyl donor having a p-trifluoromethylbenzylthio-p-trifluoromethylphenyl formimidate function as a leaving group is easily prepared by the addition of anomeric hydroxyl group of 2,3,4,6-tetra-O-benzoyl-α,β-D-glucopyranose to p-trifluoromethylphenyl isothiocyanate, followed by treatment with p-trifluoromethylbenzyl bromide. Catalytic and stereoselecrive glycosylation using this glycosyl donor effectively proceeds by activating its nitorogen atom with various protic and Lewis acids.
