740792-70-5 Usage
General Description
[ethyl(methyl)amino]acetic acid, also known as N-methyl-N-(2-acetylaminoethyl)glycine, is a chemical compound with the formula C6H12N2O3. It is classified as an amino acid derivative and functions as an analgesic and anti-inflammatory drug. It is commonly used to relieve pain associated with conditions such as osteoarthritis and rheumatoid arthritis. The compound works by inhibiting the synthesis of prostaglandins, which are lipid compounds that promote inflammation and pain. [ethyl(methyl)amino]acetic acid is typically administered orally and its effects are usually seen within 1-2 hours of ingestion. It is considered a safe and well-tolerated medication when used as directed, but like any medication, it may have potential side effects and interactions with other drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 740792-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,0,7,9 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 740792-70:
(8*7)+(7*4)+(6*0)+(5*7)+(4*9)+(3*2)+(2*7)+(1*0)=175
175 % 10 = 5
So 740792-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-3-6(2)4-5(7)8/h3-4H2,1-2H3,(H,7,8)
740792-70-5Relevant articles and documents
TRPV1 agonist, preparation method and application thereof
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Paragraph 0153-0157, (2021/03/31)
The present invention relates to a compound represented by a formula I, a stereoisomer, a tautomer, a solvate, a polymorph or a pharmaceutically acceptable salt thereof, a pharmaceutical composition containing the compound, and a preparation method and a medical use of the compound, wherein the structure of the formula I is shown in the specification.
Synthesis of N-alkyl-N-methyl amino acids. Scope and limitations of base-induced N-alkylation of Cbz-amino acids
Stodulski, Maciej,Mlynarski, Jacek
, p. 970 - 975 (2008/09/21)
The reaction of N-benzyloxycarbonyl derivatives of aliphatic amino acids with NaH/alkyl iodides gave the corresponding N-Cbz-N-alkyl derivatives in good to high yields. The scope and limitations of this simple N-alkylation reaction were investigated as a convenient and flexible attempt to prepare unsymmetrically N,N-diprotected α-amino acids. The procedure is based on the N-alkylation of N-carbamoyl amino acids, a one-pot deprotection/protection sequence without extensive purification of the products. Protection of the carboxyl function is not required while the starting materials are inexpensive and commercially available.
