720655-67-4 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The IUPAC name is a systematic method of naming chemical compounds, providing a unique name for each substance.
Explanation
Amino alcohols are organic compounds containing both an amino group (-NH2) and a hydroxyl group (-OH) attached to a carbon chain.
Explanation
Stereoisomers are molecules with the same molecular formula and sequence of bonded atoms but different spatial arrangements of atoms.
Explanation
A chiral molecule is one that cannot be superimposed on its mirror image, resulting in two non-superimposable mirror-image forms called enantiomers.
Explanation
The compound has various applications in the chemical and pharmaceutical industries, including the synthesis of new compounds and materials.
Explanation
The compound may have biological properties that could be exploited in the development of new therapeutic agents.
Explanation
Due to its properties and potential uses, it is essential to handle the compound carefully to minimize risks associated with exposure or accidental ingestion.
Classification
Amino alcohol
Stereoisomers
Four
Chirality
(1S,3S,4R,6S) form is a chiral molecule
Applications
Synthesis of pharmaceuticals, building block for organic compounds, potential use in polymers and resins production
Biological activity
Potential use in research and development of new drugs or medical treatments
Safety
Handle and use with caution, following proper safety protocols and guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 720655-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,0,6,5 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 720655-67:
(8*7)+(7*2)+(6*0)+(5*6)+(4*5)+(3*5)+(2*6)+(1*7)=154
154 % 10 = 4
So 720655-67-4 is a valid CAS Registry Number.
720655-67-4Relevant academic research and scientific papers
Enzymatic desymmetrization of 2,5-dideoxystreptamine precursors
Chenevert, Robert,Jacques, Frederic
, p. 1017 - 1021 (2007/10/03)
The stereoselective enzymatic acylation of meso-6,7-diazabicyclo[3.2.1]oct-6-ene-2,4-diol 4 and meso-4,6-diazidocyclohexane-1,3-diol 5 in organic media gave the corresponding monoesters in high enantiomeric excess. The hydrolysis of the corresponding diac
Total synthesis of 2,5-dideoxystreptamines
-
, (2008/06/13)
The dextrorotatory and levorotatory isomers of 1,6-Carbamate-3N-carbethoxy-2,5-dideoxystreptamine (I) have been found to be very valuable intermediates useful in the preparation of totally synthetic aminoglycoside antibiotics. An example of such an aminoglycoside antibiotic is 5-deoxykanamycin A.
Process for the preparation of 2,5-dideoxystreptamine and of a novel intermediate therefor
-
, (2008/06/13)
The aminocyclitol 2,5-dideoxystreptamine may be prepared by a novel two-step synthesis from cis-4,8-dioxatricyclo [5.1.0.03,5 ]octane. The aminocyclitol and a novel intermediate in the synthesis thereof are utilized by a Micromonospora inyoensis (M. inoyensis strain 155OF-1G NRRL 5742) for the elaboration of a novel antibacterial agent designated Mutamicin 2.
Synthesis of cis-1,4-cyclohexadiene dioxide
-
, (2008/06/13)
Cis-1,4-cyclohexadiene dioxide is a valuable intermediate useful in the preparation of totally synthetic aminoglycosides. An example of such an aminoglycoside is 5-deoxykanamycin A.
2,5-Dideoxystreptamine and the production thereof
-
, (2008/06/13)
2,5-Dideoxystreptamine is provided which is a new compound useful in the fermentative production of 5-deoxyneamine having useful antibacterial activity by culturing a microorganism. The production of 2,5-dideoxystreptamine is made by catalytic hydrogenation of 6,7-diaza-bicyclo[3.2.1]octane-2,4-diol which is also a new compound.
