753008-40-1 Usage
Explanation
This is the full name of the chemical compound, which includes its structure and stereochemistry.
2. Cyclopentane Ring
Explanation
The compound has a five-membered carbon ring, which is a common structural feature in many organic compounds.
3. Phenylmethoxy Group
Explanation
A phenylmethoxy group is attached to one of the carbon atoms in the cyclopentane ring. This group consists of a benzene ring (phenyl) connected to a methoxy group (-OCH3).
4. Chiral Compound
Explanation
The compound is chiral, meaning it has a non-superimposable mirror image. This results in four possible stereoisomers due to the presence of four stereocenters.
Explanation
The stereochemistry of the compound is defined by the (1R,2S,3R,4R) configuration, which describes the spatial arrangement of the atoms at each stereocenter.
Explanation
Due to its unique structure, the compound may serve as a building block in the synthesis of pharmaceuticals or other biologically active compounds.
7. Biological Activities
Explanation
The compound may exhibit various biological activities and pharmacological properties, although further research is needed to fully understand its potential uses and applications.
Explanation
Further research is required to explore the full potential of this chemical compound, its applications, and its effects on biological systems.
Stereochemistry
(1R,2S,3R,4R)-rel
Potential Applications
Pharmaceutical Synthesis
Research Status
Ongoing
Check Digit Verification of cas no
The CAS Registry Mumber 753008-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,3,0,0 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 753008-40:
(8*7)+(7*5)+(6*3)+(5*0)+(4*0)+(3*8)+(2*4)+(1*0)=141
141 % 10 = 1
So 753008-40-1 is a valid CAS Registry Number.
753008-40-1Relevant academic research and scientific papers
Synthesis and binding properties of cyclopentane analogues of myo-inositol 1,4,5-tris(phosphate)
Moris, Marc-Antoine,Caron, Annabelle Z.,Guillemette, Gaetan,Schlewer, Gilbert
, p. 3995 - 4001 (2007/10/03)
Cyclopentanic analogues of myo-inositol 1,4,5-tris(phosphate) were synthesised starting from cyclopentadiene. The affinities of the trisphosphorylated derivatives for the Ins(1,4,5)P3 receptors were equipotent to that of compound 4, showing that the relative orientation of the functional groups, particularly of the hydroxyl, is not of prime importance in this series. The 31P NMR titration curves show that the tris(phosphate) 5 behaves as the superimposition of an independent phosphate and a vicinal bis(phosphate).
