13062-76-5 Usage
Description
4-[2-(Methylamino)ethyl]phenol hydrochloride, also known as methylamphetamine hydrochloride, is an organic compound with a chemical structure that features a phenol group and a methylaminoethyl side chain. It is an off-white solid and is commonly used in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
4-[2-(Methylamino)ethyl]phenol hydrochloride is used as an active pharmaceutical ingredient for its stimulant properties. It is known to stimulate pancreatic exocrine secretion via the cholinergic gastropancreatic reflex, which can be beneficial in treating certain medical conditions related to pancreatic function.
Used in Beverage Industry:
In the beverage industry, particularly in the production of beer, 4-[2-(Methylamino)ethyl]phenol hydrochloride is used as a component to enhance the taste and quality of the final product. Its stimulant properties can contribute to the overall experience of consuming the beverage, making it more appealing to consumers.
Used in Chemical Research:
4-[2-(Methylamino)ethyl]phenol hydrochloride is also utilized in chemical research as a starting material or intermediate for the synthesis of various other organic compounds. Its unique structure and properties make it a valuable tool in the development of new chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 13062-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13062-76:
(7*1)+(6*3)+(5*0)+(4*6)+(3*2)+(2*7)+(1*6)=75
75 % 10 = 5
So 13062-76-5 is a valid CAS Registry Number.
13062-76-5Relevant articles and documents
Cactus alkaloids. X. Isolation of hordenine and N-methyltyramine from Ariocarpus kotschoubeyanus.
Neal,Sato,Johnson,McLaughlin
, p. 477 - 478 (1971)
-
Catalytic Strategy for Regioselective Arylethylamine Synthesis
Boyington, Allyson J.,Seath, Ciaran P.,Zearfoss, Avery M.,Xu, Zihao,Jui, Nathan T.
supporting information, p. 4147 - 4153 (2019/03/07)
A mild, modular, and practical catalytic system for the synthesis of the highly privileged phenethylamine pharmacophore is reported. Using a unique combination of organic catalysts to promote the transfer of electrons and hydrogen atoms, this system performs direct hydroarylation of vinyl amine derivatives with a wide range of aryl halides (including aryl chlorides). This general and highly chemoselective protocol delivers a broad range of arylethylamine products with complete regiocontrol. The utility of this process is highlighted by its scalability and the modular synthesis of an array of bioactive small molecules.
Total synthesis and biological evaluation of methylgerambullone
Moon, Jong Taik,Ha, Sung Hoon,Lee, So Hyung,Kwon, Tae Hui,Oh, Chun Rim,Kim, Young Deuk,Kim, Jungahn,Choo, Dong Joon,Lee, Jae Yeol
scheme or table, p. 52 - 55 (2010/04/24)
First total synthesis of methylgerambullone (MGB, 1) isolated from Glycosmis angustifolia was completed via a convergent route. The effect of MGB on the contractile responses of the isolated guinea-pig ileum induced by acetylcholine was investigated. As a result, it showed a potent relaxation rate (78.66 ± 4.30% at 100 mg/L) in a concentration-dependent manner on longitudinal smooth muscle contraction of isolated guinea-pig ileum induced by 1 μM acetylcholine.
