127003-34-3 Usage
Molecular structure
The compound has a complex structure consisting of a 1-propanamine core, a 2-phenoxy group, a 2-(4-chlorophenyl)ethyl group, and an N,N-dimethyl group.
Functional groups
The presence of amine (-NH2), phenoxy (-OC6H4), and dimethylamino (-N(CH3)2) groups contribute to its reactivity and potential applications.
Substitution pattern
The chlorine atom is attached to the phenyl ring at the para position (4-chlorophenyl), which may influence the compound's properties and reactivity.
Physical state
The compound is likely a solid at room temperature, as many organic compounds with similar structures and molecular weights are.
Industrial and pharmaceutical applications
The compound can be used as an intermediate in the synthesis of other compounds or as a component in the production of pharmaceuticals or other organic materials.
Versatility
Due to its complex structure and multiple functional groups, the compound may have a wide range of potential uses depending on the specific context in which it is being considered.
Reactivity
The presence of various functional groups, such as the amine and phenoxy groups, may make the compound reactive with other chemicals, allowing for further modification or synthesis of new compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 127003-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,0 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127003-34:
(8*1)+(7*2)+(6*7)+(5*0)+(4*0)+(3*3)+(2*3)+(1*4)=83
83 % 10 = 3
So 127003-34-3 is a valid CAS Registry Number.
127003-34-3Relevant academic research and scientific papers
Syntheses and Platelet Aggregation Inhibitory and Antithrombotic Properties of ethyl>benzenes
Kikumoto, Ryoji,Hara, Hiroto,Ninomiya, Kunihiro,Osakabe, Masanori,Sugano, Mamoru,et al.
, p. 1818 - 1823 (2007/10/02)
A series of ethyl>benzene derivatives were synthesized and evaluated for their ability to inhibit collagen-induced platelet aggregation in vitro and to protect experimantal thrombosis in mice.The results showed that the compounds were in vitro inhibitors of collagen-induced platelet aggregation.Most of them were also effective in the mouse antithrombotic assay.The compounds were found to be potent antagonists to S2 serotonergic receptor, and good correlation (r = 0.85) between their S2 serotonergic receptor antagonism and their potency as platelet antiaggregatory drugs was observed.Among the compounds studied, monophenoxy>methyl>ethyl>succinate hydrochloride (12b, MCI-9042) was selected for further pharmacological and toxicological evaluation.
Pharmaceutically active (omega-aminoalkoxy)bibenzyls
-
, (2008/06/13)
(Omega-aminoalkoxy)bibenzyls are prepared and found useful as pharmaceutical agents, particularly as inhibitors of platelet aggregation.
