4152-81-2 Usage
Chemical compound
A substance with a specific molecular structure that is formed by a chemical reaction.
Complex structure
The compound has a pentofuranose ring with acetyl and benzoyl functional groups attached to it.
Acetyl functional groups
These are derived from acetic acid and are characterized by the presence of a carbonyl group (C=O) and a methyl group (CH3).
Benzoyl functional groups
These are derived from benzoic acid and consist of a carbonyl group (C=O) attached to a benzene ring.
Pentofuranose ring
A five-membered ring structure composed of four carbon atoms and one oxygen atom.
Deoxy sugar
A sugar molecule with one or more hydroxyl (OH) groups replaced by hydrogen atoms, resulting in a lack of an oxygen atom.
Hydroxyl groups
These are functional groups consisting of an oxygen atom bonded to a hydrogen atom (OH).
High level of complexity
The presence of multiple functional groups and the deoxy sugar nature of the compound contribute to its complexity.
Research and industrial applications
The compound is suitable for use in various research and industrial applications, particularly in organic chemistry and the synthesis of complex molecules.
Organic chemistry
A branch of chemistry that focuses on the study of carbon-containing compounds and their reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 4152-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,5 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4152-81:
(6*4)+(5*1)+(4*5)+(3*2)+(2*8)+(1*1)=72
72 % 10 = 2
So 4152-81-2 is a valid CAS Registry Number.
4152-81-2Relevant academic research and scientific papers
First total synthesis of a naturally occurring iodinated 5′-deoxyxylofuranosyl marine nucleoside
Sun, Jianyun,Dou, Yanhui,Ding, Haixin,Yang, Ruchun,Sun, Qi,Xiao, Qiang
, p. 881 - 889 (2012/07/14)
4-Amino-7-(5′-deoxy-β-D-xylofuranosyl)-5-iodo-pyrrolo[2,3-d] pyrimidine 1, an unusual naturally occurring marine nucleoside isolated from an ascidan, Diplosoma sp., was synthesized from D-xylose in seven steps with 28% overall yield on 10 g scale. The key step was Vorbrueggen glycosylation of 5-iodo-pyrrolo[2,3-d]pyrimidine with 5-deoxy-1, 2-O-diacetyl-3-O-benzoyl-D- xylofuranose. Its absolute configuration was confirmed.
