What is the 2',3',5'-TRI-O-BENZOYLINOSINE?

2',3',5'-TRI-O-BENZOYLINOSINE is , while it's Molecular Formula is C31H24 N4 O8. Used in Pharmaceutical Industry: 2',3',5'-Tri-O-benzoylinosine is used as a precursor in the synthesis of nucleoside analogs for the development of antiviral, anticancer, and antiparasitic drugs. The benzoyl modification increases its reactivity, allowing for the introduction of other chemical groups and enhancing its potential therapeutic applications. Used in Organic Synthesis: 2',3',5'-Tri-O-benzoylinosine is used as a building block in organic synthesis due to its enhanced reactivity and stability. The presence of benzoyl groups at the 2', 3', and 5' positions makes it a versatile intermediate for the preparation of various nucleoside derivatives with potential applications in medicinal chemistry and drug development.

What is the CAS number for 2',3',5'-TRI-O-BENZOYLINOSINE?

The CAS number of 2',3',5'-TRI-O-BENZOYLINOSINE is 6741-88-4.

What is 2',3',5'-TRI-O-BENZOYLINOSINE (6741-88-4) used for?

2',3',5'-Tri-O-benzoylinosine is a chemical compound derived from inosine, a nucleoside present in RNA with various biological functions. It is modified by the addition of benzoyl groups at the 2', 3', and 5' positions, which enhances its reactivity and stability, making it a valuable precursor in the synthesis of nucleoside derivatives and a promising candidate for the development of antiviral, anticancer, and antiparasitic agents.

What is the 2',3',5'-TRI-O-BENZOYLINOSINE?

2',3',5'-TRI-O-BENZOYLINOSINE is , while it's Molecular Formula is C31H24 N4 O8. Used in Pharmaceutical Industry: 2',3',5'-Tri-O-benzoylinosine is used as a precursor in the synthesis of nucleoside analogs for the development of antiviral, anticancer, and antiparasitic drugs. The benzoyl modification increases its reactivity, allowing for the introduction of other chemical groups and enhancing its potential therapeutic applications. Used in Organic Synthesis: 2',3',5'-Tri-O-benzoylinosine is used as a building block in organic synthesis due to its enhanced reactivity and stability. The presence of benzoyl groups at the 2', 3', and 5' positions makes it a versatile intermediate for the preparation of various nucleoside derivatives with potential applications in medicinal chemistry and drug development.

What is the CAS number for 2',3',5'-TRI-O-BENZOYLINOSINE?

The CAS number of 2',3',5'-TRI-O-BENZOYLINOSINE is 6741-88-4.

What is 2',3',5'-TRI-O-BENZOYLINOSINE (6741-88-4) used for?

2',3',5'-Tri-O-benzoylinosine is a chemical compound derived from inosine, a nucleoside present in RNA with various biological functions. It is modified by the addition of benzoyl groups at the 2', 3', and 5' positions, which enhances its reactivity and stability, making it a valuable precursor in the synthesis of nucleoside derivatives and a promising candidate for the development of antiviral, anticancer, and antiparasitic agents.

2',3',5'-TRI-O-BENZOYLINOSINE

Quality Factory Supply 99% Pure 2',3',5'-TRI-O-BENZOYLINOSINE 6741-88-4 with Efficient Delivery

Molecular Formula: C31H24 N4 O8
Molecular Weight: 580.554
PSA： 151.96000
LogP: 3.73750

6741-88-4 Relevant articles

High-throughput five minute microwave accelerated glycosylation approach to the synthesis of nucleoside libraries

Bookser, Brett C.,Raffaele, Nicholas B.

, p. 173 - 179 (2007/10/03)

The Vorbrueggen glycosylation reaction w...

Synthesis and stability of GNRA-loop analogs

Woerner, Karlheinz,Strube, Thorsten,Engels, Joachim W.

, p. 2094 - 2104 (2007/10/03)

Nebularinc, 9-(β-D-ribofuranosyl)-9H-pur...

Oxidative Transformations of Minor Components of Nucleic Acids. An Anomalous Reaction Course of Oxidation of N6,N6-Dialkyladenosines and Related Compounds with m-Chloroperoxybenzoic Acid

Endo, Takeshi,Zemlicka, Jiri

, p. 1887 - 1894 (2007/10/02)

Oxidation of N6-methyladenosine (1a) or ...

The preparation of 14C-Labeled Ribosyl-trans-zeatin and Its cis Isomer

Nakajima, Hiromitsu,Yokota, Takao,Watanabe, Naoharu,Takahashi, Nobutaka

, p. 2717 - 2720 (2007/10/02)

14C-Labeled ribosyl-trans-zeatin and its...

6741-88-4 Process route

: 71118-15-5
C₃₆H₃₃N₅O₇

: 6741-88-4
2',3',5'-tri-O-benzoylinosine

Conditions

Conditions	Yield
With 3-chloro-benzenecarboperoxoic acid; In chloroform; Ambient temperature;	57%

: 16645-06-0
N,N-dimethylhydroxylamine hydrochloride

: 3510-73-4,179112-79-9
(2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(6-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl dibenzoate

: 70230-70-5
N⁶,N⁶-dimethyladenosine tribenzoate

: 6741-88-4
2',3',5'-tri-O-benzoylinosine

Conditions

Conditions	Yield
With triethylamine; In N,N-dimethyl-formamide; for 30h; Ambient temperature;	76% 13%

6741-88-4 Upstream products

98-88-4
benzoyl chloride
70230-70-5
N⁶,N⁶-dimethyladenosine tribenzoate
71118-13-3
C₃₅H₃₃N₅O₇
71118-15-5
C₃₆H₃₃N₅O₇

6741-88-4 Downstream products

6741-90-8
2',3',5'-tri-O-benzoyl-6-thioinosine
574-25-4
6-thioinosine
151132-93-3
9-[5'-O-(4,4'-dimethoxytriphenylmethyl)-β-D-ribofuranosyl]-9H-purine
151132-94-4
9-{5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-[(tert-butyl)dimethylsilyl]-β-D-ribofuranosyl}-9H-purine