51319-18-7 Usage
Type of compound
Sympathomimetic amine
Common uses
Decongestant, bronchodilator, stimulant, appetite suppressant, precursor in the manufacture of methamphetamine
Chirality
Chiral compound with two enantiomers
Natural sources
Found in various botanical sources such as the Ephedra plant
Mechanism of action
Non-selective agonist of the adrenergic receptors, leading to increased heart rate, vasoconstriction, and increased blood pressure
Legal status
Controlled substance in many countries due to potential for abuse and adverse cardiovascular effects.
Check Digit Verification of cas no
The CAS Registry Mumber 51319-18-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,1 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51319-18:
(7*5)+(6*1)+(5*3)+(4*1)+(3*9)+(2*1)+(1*8)=97
97 % 10 = 7
So 51319-18-7 is a valid CAS Registry Number.
51319-18-7Relevant articles and documents
Solvent-Directed Epoxide Opening with Primary Amines for the Synthesis of β-Amino Alcohols
Lizza, Joseph R.,Moura-Letts, Gustavo
supporting information, p. 1231 - 1242 (2017/03/11)
An efficient synthesis of β-amino alcohols from a variety of epoxides and primary unbranched amines in the absence of any catalyst in high yields and regioselectivities is reported. A variety of polar mixed solvent systems allow for the selective formation of secondary amino alcohols over tertiary amino alcohols. The reaction scope extends to a wide variety of aromatic and aliphatic substituted epoxides and primary amines bearing complex functionality.
Stereospecific preparation of (3S,4R,5R)-3-(1-hydroxyethyl)-4-benzoyloxy-azeridinones from L-(-)-theonine
-
, (2008/06/13)
Azetidinones represented by the formula STR1 are prepared by a multistep process from L-(-)-theonine via an epoxyamide.
