4360-62-7 Usage
Physical state
Colorless liquid
The compound's appearance and state of matter at room temperature.
Applications
Pharmaceutical synthesis, organic compounds
Bromophenylmethyl group
Potential applications in drug development
The specific functional group within the compound that may contribute to its use in creating new drugs and therapeutic agents.
Building block
Organic synthesis
The compound's role as a fundamental component in the creation of various pharmaceutical and research compounds.
Health risks
Handle with caution
A warning that the compound may pose health risks if not handled properly, emphasizing the need for safety precautions during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 4360-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4360-62:
(6*4)+(5*3)+(4*6)+(3*0)+(2*6)+(1*2)=77
77 % 10 = 7
So 4360-62-7 is a valid CAS Registry Number.
4360-62-7Relevant articles and documents
Structure and thermal reactivity of some 2-substituted 1,3-oxathiolane S-oxides
Aitken, R. Alan,Henderson, Sarah,Slawin, Alexandra M. Z.
, p. 422 - 434 (2018/03/26)
Isomerization of 2-benzylidene-1,3-dioxolane to 3-phenylbutyrolactone occurs readily under flash vacuum pyrolysis (FVP) conditions. 2-Diphenylmethyl-1,3-oxathiolane and 2-benzyl-1,3-oxathiolane have been prepared and the latter compound has been oxidized to the corresponding sulfoxide, whose structure and conformation are examined by 1H NMR, and to the sulfone whose X-ray structure is determined. 2-Benzylidene-1,3-oxathiolane is also prepared and the behavior of the three S-oxidized oxathiolane derivatives upon FVP is examined. While extrusion of SOn to give ethene and a carbonyl compound predominates in all three cases, the sulfoxide gives also bis(2-hydroxyethyl) disulfide, most likely formed via thiirane S-oxide and 1,2-oxathietane.
