114379-44-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 16 carbon (C) atoms, 35 hydrogen (H) atoms, 1 nitrogen (N) atom, and 3 oxygen (O) atoms.
Explanation
Amino alcohols are organic compounds that contain both an amine (-NH2) group and an alcohol (-OH) group. This compound has an amine group at the 2nd carbon and three hydroxyl (-OH) groups at the 1st, 3rd, and 4th carbons.
Explanation
The stereochemical configuration describes the spatial arrangement of atoms in a molecule. In this case, the (2S,3S,4R) designation indicates that the hydroxyl groups at the 2nd and 3rd carbons are in the "S" (si) configuration, while the hydroxyl group at the 4th carbon is in the "R" (rectus) configuration.
Explanation
This compound is commonly used in the synthesis of pharmaceuticals and organic compounds. It may also have potential applications in the development of new drugs or research into biological processes. Additionally, it may have uses in various industrial processes, such as in the production of polymers or as a component in chemical reactions.
Explanation
The compound contains an amino group at the 2nd carbon and three hydroxyl groups at the 1st, 3rd, and 4th carbons. These functional groups contribute to the compound's reactivity and its ability to form various products in chemical reactions.
Explanation
The solubility of this compound is not provided in the material, but it would depend on the solvent used. Amino alcohols generally have varying solubility in different solvents, such as water, alcohols, or organic solvents.
Explanation
The stability of this compound is not provided in the material, but it would depend on factors such as temperature, pressure, and the presence of other reactive substances. Amino alcohols can be sensitive to certain conditions, so it is essential to consider these factors when handling or storing the compound.
Type of Compound
Amino Alcohol
Stereochemical Configuration
(2S,3S,4R)
Applications
Pharmaceutical Synthesis, Organic Compounds, Drug Development, Biological Research, Industrial Processes
Functional Groups
Amino Group (-NH2), Hydroxyl Groups (-OH)
Solubility
Unknown (depends on solvent)
Stability
Unknown (depends on conditions)
Check Digit Verification of cas no
The CAS Registry Mumber 114379-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,7 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 114379-44:
(8*1)+(7*1)+(6*4)+(5*3)+(4*7)+(3*9)+(2*4)+(1*4)=121
121 % 10 = 1
So 114379-44-1 is a valid CAS Registry Number.
114379-44-1Relevant articles and documents
Agelasphins, novel antitumor and immunostimulatory cerebrosides from the marine sponge Agelas mauritianus
Natori, Takenori,Morita, Masahiro,Akimoto, Kohji,Koezuka, Yasuhiko
, p. 2771 - 2784 (2007/10/02)
New glycosphingolipids, named agelasphins (1-8), have been isolated by antitumor and immunostimulatory bioassay-guided purification from an extract of a marine sponge, Agelas mauritianus. Strongly active agents in agelasphins had characteristic α-galactosylceramide structures, the isolation of which from natural products has not previously been reported. The absolute configurations of agelasphins were elucidated by the total synthesis.
