1367567-95-0 Usage
Description
Phenylephrine EP Impurity D, also known as (αR)-3-Hydroxy-α-[[methyl(phenylmethyl)amino]methyl]-benzenemethanol, is a derivative of (R)-Phenylephrine (P320640, HCl salt). It is an α-Adrenergic agonist, which means it has the ability to bind to and activate α-adrenergic receptors in the body.
Uses
Phenylephrine EP Impurity D is used as a pharmaceutical compound for its α-adrenergic agonist properties. It is particularly useful in the development and testing of medications that target α-adrenergic receptors, which play a crucial role in various physiological processes, including vasoconstriction, blood pressure regulation, and neurotransmission.
Used in Pharmaceutical Industry:
Phenylephrine EP Impurity D is used as a reference compound for the development and quality control of medications containing (R)-Phenylephrine. Its presence in the pharmaceutical industry is essential for ensuring the safety, efficacy, and purity of α-adrenergic agonist drugs.
Used in Research and Development:
Phenylephrine EP Impurity D is used as a research tool in the study of α-adrenergic receptors and their role in various physiological processes. It can help researchers understand the mechanisms of action, potential side effects, and therapeutic applications of α-adrenergic agonist drugs.
Used in Quality Control and Regulatory Compliance:
Phenylephrine EP Impurity D is used as a reference material in the quality control and regulatory compliance processes of pharmaceutical manufacturers. It helps ensure that the final drug products meet the required standards for purity, potency, and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 1367567-95-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,7,5,6 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1367567-95:
(9*1)+(8*3)+(7*6)+(6*7)+(5*5)+(4*6)+(3*7)+(2*9)+(1*5)=210
210 % 10 = 0
So 1367567-95-0 is a valid CAS Registry Number.
1367567-95-0Relevant articles and documents
Chiral amino-pyridine-phosphine tridentate ligand, manganese complex, and preparation method and application thereof
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Paragraph 0597-0600; 0603, (2020/07/13)
The invention discloses a chiral amino-pyridine-phosphine tridentate ligand, a manganese complex, and a preparation method and application thereof. The chiral amino-pyridine-phosphine tridentate ligand is shown as a formula II, and the manganese complex of the chiral amino-pyridine-phosphine tridentate ligand can be used for efficiently catalyzing and hydrogenating ketone compounds to prepare chiral alcohol compounds in a high enantioselectivity mode. The chiral amino-pyridine-phosphine tridentate ligand and the manganese complex are simple in synthesis process, good in stability, high in catalytic activity and mild in reaction conditions.
Method for Ir/f-amphox high-efficiency synthesis of chiral α- C-amino alcohol by virtue of catalytic oxidation 1,2- of P-aminoketone by using one-aminoketone
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Paragraph 0073-0078, (2020/01/03)
The invention discloses a method for efficiently synthesizing chiral 1,2-amino alcohol by catalyzing alpha-aminoketone through Ir/f-amphox. A ligand f-amphox used by the method can be more easily synthesized; the reaction has the characteristics of enanti
Method for preparing of L-phenylephrine hydrochloride
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, (2008/06/13)
The present invention relates to an improved process for preparing L-phenylephrine hydrochloride 3 on an industrial scale by asymmetric hydrogenation as the key step and a special sequence of subsequent steps, using [Rh(COD)Cl]2 as catalyst and a chiral, two-pronged phosphine ligand such as (2R,4R)-4-(dicyclohexylphosphino)-2-(diphenylphosphino-methyl)-N-methyl-aminocarbonyl-pyrrolidine as the catalyst system.
