4688-34-0 Usage
Chemical structure
A dithione derivative with two morpholine groups attached to a central ethane chain
Functional groups
Dithione, morpholine, and ethane
Applications
a. Cross-linking agent in the synthesis of polymers
b. Reagent in organic synthesis
c. Potential application in the development of new materials and pharmaceuticals
Importance
An important intermediate in the field of organic chemistry
Industrial uses
Potential uses in various industries due to its versatility as a cross-linking agent and reagent
Research focus
Studies on its potential application in material development and pharmaceuticals
Chemical properties
a. Reactivity with other compounds for cross-linking and organic synthesis
b. Stability in various reaction conditions
Physical properties
a. Appearance (likely a solid or liquid, depending on the conditions)
b. Solubility (likely soluble in organic solvents)
c. Melting or boiling point (specific values would depend on the compound's structure and molecular weight)
Safety and handling
As with any chemical compound, appropriate safety measures should be taken when handling 1,2-di(morpholin-4-yl)ethane-1,2-dithione, including the use of personal protective equipment and proper disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 4688-34-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4688-34:
(6*4)+(5*6)+(4*8)+(3*8)+(2*3)+(1*4)=120
120 % 10 = 0
So 4688-34-0 is a valid CAS Registry Number.
4688-34-0Relevant academic research and scientific papers
A domino annulation reaction under Willgerodt-Kindler conditions
Kadzimirsz, Daniel,Kramer, Daniel,Sripanom, Lertnarong,Oppel, Iris M.,Rodziewicz, Pawel,Doltsinis, Nikos L.,Dyker, Gerald
, p. 4644 - 4649 (2008/09/21)
(Chemical Equation Presented) Butanone side chains at arenes and hetarenes, efficiently introduced by a Heck-type reaction, are transformed to annulated thieno[3,2-b]thiophenes in a domino redox process under Willgerodt-Kindler conditions. A nucleophilic aromatic substitution with an intermediary thioenolate is a reasonable key step of this process.
POTENTIAL ANTIDEPRESSANT AND ANTI-INFLAMMATORY AGENTS: 4-(2-PROPYLTHIO)ACETOPHENONE OXIMES AND 4-(2-PROPYLTHIO)PHENYLALKANOIC ACIDS
Jilek, Jiri,Sindelar, Karel,Grimova, Jaroslava,Maturova, Eva,Holubek, Jiri,et al.
, p. 1266 - 1277 (2007/10/02)
4-(2-Propylthio)acetophenone oxime (IV) was reacted with 2-aminoethyl chloride and 3-dimethylaminopropyl chloride to give the O-(aminoalkyl)oximes V and VI which are analogues of the antidepressant agent fluvoxamine (I).Kindler-Willgerodt reaction of 4-(2
