56579-84-1 Usage
Chemical Family
Dithiane family
Type of Compound
Ester of 1,3-dithiane-2-carboxylic acid
Common Use
Building block in organic synthesis
Reactions
Ability to undergo reactions with various electrophiles
Result of Reactions
Formation of diverse functionalized compounds
Protective Group
Utilized as a protective group for aldehydes and ketones in organic synthesis
Application
Used in the preparation of pharmaceuticals and agrochemicals
Anti-cancer Properties
Studied for its anti-cancer properties
Potential
Potential as a drug candidate for the treatment of various types of cancer
Check Digit Verification of cas no
The CAS Registry Mumber 56579-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56579-84:
(7*5)+(6*6)+(5*5)+(4*7)+(3*9)+(2*8)+(1*4)=171
171 % 10 = 1
So 56579-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2S2/c1-8-5(7)6-9-3-2-4-10-6/h6H,2-4H2,1H3
56579-84-1Relevant academic research and scientific papers
STUDY OF THE ANOMERIC EFFECT IN 2-SUBSTITUTED 1,3-DITHIANES
Juaristi, Eusebio,Tapia, Josefina,Mendez, Rodolfo
, p. 1253 - 1264 (2007/10/02)
The conformational analysis of several 2-substituted 1,3-dithianes made possible the evaluation of S-C-Y anomeric interactions, where Y=SCH3,SC6H5,CO2CH3,COC6H5,CO2H and N(CH3)2.The relative magnitude of the effects observed for these groups odithiane(Y)-ΔGocyclohexane(Y)> can be explained in terms of the combined influence of dipole/dipole and two-electron stabilizing interactions (stereoelectronic effect).
1-Carba-6-(1-hydroxyethyl)-2-carbonyl-penem-3-carboxylic acid and preparation thereof
-
, (2008/06/13)
Antibiotic 1-carba-6-(1-hydroxyethyl-2-carbonyl-penem-3-carboxylic acid is prepared by total chemical synthesis from 4-iodomethyl-1-(t-butyldimethylsilyl)-2-azetidinone.
