150617-83-7 Usage
Structure
Tetrahydroxy derivative of cyclopentane The compound consists of a five-membered ring with four hydroxyl (OH) groups attached to it.
Stereochemistry
(1R,2R,3S,4S)-rel-(9CI) The compound has a specific three-dimensional arrangement of its atoms, with the hydroxyl groups at the 1, 2, 3, and 4 positions having R, R, S, and S configurations, respectively.
Applications
Organic synthesis and material science 1,2,3,4-Cyclopentanetetramethanol can be used as a building block for the synthesis of complex organic molecules or as a precursor for the production of polymeric materials.
Industrial and research value
Unique structure and properties The compound's structure and properties make it a valuable chemical for various industrial and research purposes.
Potential pharmaceutical applications
Further research and testing needed While 1,2,3,4-Cyclopentanetetramethanol may have potential medical uses, additional research and testing are necessary to explore these possibilities.
Check Digit Verification of cas no
The CAS Registry Mumber 150617-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,1 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150617-83:
(8*1)+(7*5)+(6*0)+(5*6)+(4*1)+(3*7)+(2*8)+(1*3)=117
117 % 10 = 7
So 150617-83-7 is a valid CAS Registry Number.
150617-83-7Relevant articles and documents
A new tetratertiary phosphine ligand and its use in Pd-catalyzed allylic substitution
Laurenti,Feuerstein,Pepe,Doucet,Santelli
, p. 1633 - 1637 (2007/10/03)
A new tetraphosphine, the cis-cis-cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane (Tedicyp) 1 has been synthesized, characterized, and used in Pd-catalyzed allylic substitutions. The Tedicyp was easily prepared in seven steps from the commercially available himic anhydride. The structure of the complex Tedicyp-borane was determined by X-ray analysis. The tetraphosphine in combination with [Pd(η3-C3H5)Cl]2 affords a very efficient catalyst for allylic substitution of several allylic acetates. Under mild conditions, very high turnover numbers and turnover frequencies have been obtained.
