72033-44-4 Usage
Chemical compound
A substance formed by a chemical reaction, with a specific molecular structure and properties.
Complex molecular structure
The compound has a multi-part structure, consisting of various functional groups and moieties.
Indolyl group
A heterocyclic aromatic ring system derived from indole, which is a part of the compound's structure.
Amino group
A functional group containing a nitrogen atom bonded to two hydrogen atoms (-NH2), present in the compound.
Oxoethyl group
A functional group containing a carbonyl group (C=O) attached to an ethyl group (-CH2CH3), which is part of the compound.
Hexopyranuronic acid moiety
A six-carbon sugar derivative with a carboxylic acid group, which is a component of the compound.
Methyl ester functional group
An ester formed by the reaction of a carboxylic acid and methanol, which is part of the compound's structure.
Synthetic derivative
The compound is not found naturally but is created through chemical synthesis.
Potential applications
The compound may have uses in the pharmaceutical or research fields, although specific applications are not readily available.
Biological activity
The compound's complex structure suggests it may interact with biological systems, making it a potential target for further study.
Further study
The compound's properties and potential applications may warrant additional research to better understand its interactions with biological systems and possible uses.
Check Digit Verification of cas no
The CAS Registry Mumber 72033-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,3 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72033-44:
(7*7)+(6*2)+(5*0)+(4*3)+(3*3)+(2*4)+(1*4)=94
94 % 10 = 4
So 72033-44-4 is a valid CAS Registry Number.
72033-44-4Relevant articles and documents
Synthesis of the Indole Nucleoside Antibiotics Neosidomycin and SF-2140: Structural Revision of Neosidomycin
Buchanan, J. Grant,Stoddart, Jane,Wightman, Richard H.
, p. 823 - 824 (1989)
Two structurally related indole nucleoside antibiotics, neosidomycin (5) and SF-2140 (3) have been synthesised; it is confirmed that the structure initially proposed for neosidomycin must be revised.
Synthesis of the Indole Nucleoside Antibiotics Neosidomycin and SF-2140
Buchanan, J. Grant,Stoddart, Jane,Wightman, Richard H.
, p. 1417 - 1426 (2007/10/02)
The indole nucleoside antibiotics neosidomycin 5 and SF-2140 3 have been synthesized.Methyl 4-deoxy-2,3-O-isopropylidene-α-D-lyxo-hexopyranoside 8 was converted into methyl 1-chloro-1,4-dideoxy-2,3-di-O-pivaloyl-α-D-lyxo-hexopyranuronate 33 in five steps.Silver(I)-catalysed coupling of compound 33 with 3-(cyanomethyl)indole 20 gave stereoselectively an α-nucleoside which was converted into methyl 1--1,4-dideoxy-α-D-lyxo-hexopyranuronate (neosidomycin, 5).Coupling of compound 33 to 3-cyanomethyl-4-methoxyindole 23 by the sodium salt procedure, and subsequent deacylation, gave methyl 1-(3-cyanomethyl-4-methoxyindol-1-yl)-1,4-dideoxy-α-D-lyxo-hexopyranuronate (SF-2140, 3).Neosidomycin, SF-2140, and their O-acyl derivatives adopt a conformation which differs from that of 1-(6-O-benzoyl-4-deoxy-2,3-O-pivaloyl-α-D-lyxo-hexopyranosyl)-3-(cyanomethyl)indole 29, in which the methyl uronate grouping of the antibiotics is present at a lower oxidation level.
