768381-36-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound is derived from 1,3-dioxolane-4-propanol,2,2-dimethylby replacing a hydroxyl group with an acetate group.
Explanation
The stereochemistry of the compound is indicated by the (4S)-(9CI) notation, which describes the spatial arrangement of atoms around the chiral center at the 4th position.
Explanation
The compound contains an acetate group, a cyclic ether (1,3-dioxolane), and a hydroxyl group, which are the main functional groups present in the molecule.
Explanation
The compound is used in various industries, including the production of fragrances and flavors, as well as in the development of pharmaceuticals. It may also be utilized in organic synthesis and chemical research.
Explanation
The compound is likely to be soluble in organic solvents such as ethanol, methanol, and acetone due to its nonpolar nature.
Explanation
The compound is expected to be stable under normal conditions, such as room temperature and pressure, without undergoing significant decomposition or reaction.
Explanation
The compound may undergo reactions with strong acids, bases, or nucleophiles, which could lead to the formation of new products or the cleavage of functional groups.
Explanation
The compound may pose a risk of irritation or sensitization upon contact with the skin or respiratory system, and appropriate safety measures should be taken when handling it.
Explanation
To maintain the stability and safety of the compound, it should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and heat sources.
Structure
Acetate derivative of 1,3-dioxolane-4-propanol,2,2-dimethyl-
Stereochemistry
(4S)-(9CI)
Functional groups
Acetate, cyclic ether, and alcohol
Applications
Fragrances, flavors, pharmaceuticals, organic synthesis, and chemical research
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Reactivity
May react with strong acids, bases, or nucleophiles
Hazards
Potential irritant or sensitizer
Storage
Store in a cool, dry, and well-ventilated area
Check Digit Verification of cas no
The CAS Registry Mumber 768381-36-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,8,3,8 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 768381-36:
(8*7)+(7*6)+(6*8)+(5*3)+(4*8)+(3*1)+(2*3)+(1*6)=208
208 % 10 = 8
So 768381-36-8 is a valid CAS Registry Number.
768381-36-8Relevant academic research and scientific papers
A convergent synthesis of enantiopure bicyclic scaffolds through multicomponent Ugi reaction
Banfi, Luca,Basso, Andrea,Guanti, Giuseppe,Merlo, Silvia,Repetto, Claudio,Riva, Renata
, p. 1114 - 1134 (2008/09/17)
An efficient and convergent Ugi synthesis of enantiomerically pure N-acyl-2,5-disubstituted pyrrolidines was coupled with an appropriate secondary transformation to give two series of bicyclic derivatives, namely hexahydro pyrrolo-oxazocinediones and -dia
Asymmetric total synthesis of martinelline and martinellic acid
Ikeda, Shuhei,Shibuya, Masatoshi,Iwabuchi, Yoshiharu
, p. 504 - 506 (2007/10/03)
Herein, we describe the first asymmetric total synthesis of (-)-martinelline ((-)-2) and the second total synthesis of (-)-martinellic acid ((-)-1) by employing a tandem Mukaiyama-Mannich reaction/aminal cyclization as the key step. The Royal Society of C
