94231-37-5 Usage
General Description
Ethyl L-ornithine monohydrochloride is a chemical compound that belongs to the class of organic compounds known as alpha amino acids and derivatives. It is an ethyl ester derivative of L-ornithine and contains a hydrochloride salt. L-ornithine is a non-essential amino acid that plays a key role in the urea cycle, which is responsible for detoxifying ammonia in the body. ethyl L-ornithine monohydrochloride has been studied for its potential use in pharmaceuticals, particularly as a treatment for liver diseases and as a nutritional supplement to support athletic performance. Additionally, it has been investigated for its potential benefits in wound healing and tissue repair. Ethyl L-ornithine monohydrochloride is often used in research and development as a chemical reagent and is of interest for its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 94231-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,3 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94231-37:
(7*9)+(6*4)+(5*2)+(4*3)+(3*1)+(2*3)+(1*7)=125
125 % 10 = 5
So 94231-37-5 is a valid CAS Registry Number.
94231-37-5Relevant articles and documents
Diastereoselective pictet-spengler reactions of a tethered 2-aminoimidazole
Shengule, Sudhir R.,Karuso, Peter
, p. 184 - 191 (2014/03/21)
The diastereoselective Pictet-Spengler reaction of aminopropyl-2- aminoimidazole with enantiopure aldehydes has been investigated. With amino acid-derived aldehydes, anti stereochemistry is favoured, with a diastereoselectivity up to 92% achievable. The absolute stereochemistry of the products was determined through synthesis of a rigid derivative and from NMR data in combination with molecular modelling. The diastereoselectivity was shown to be dependent on the steric bulk of the amino acid side chain and independent of the nitrogen protecting group. Lewis acids catalysed the reaction but did not affect the diastereoselectivity.
CERTAIN 3-PHOSPHINYL-AMINO-2-OXO-1H-AZEPINE-1-ACETIC ACID DERIVATIVES HAVING ANTI-HYPERTENSIVE ACTIVITY
-
, (2008/06/13)
Phosphonamide substituted lactams of the formula STR1 are disclosed. These compounds are useful as hypotensive agents.