1239450-42-0 Usage
General Description
The chemical 2-benzamido-3-methoxy-3-oxopropyl benzoate is a compound with the molecular formula C21H19NO5. It is a derivative of benzoic acid and contains a benzamide group and a methoxy group. This chemical is commonly used in pharmaceutical research and drug development due to its potential pharmacological properties. It may have applications in various therapeutic areas, including anti-inflammatory, analgesic, and antipyretic activities. Furthermore, it may also exhibit antioxidant and antimicrobial properties, making it a versatile and potentially valuable chemical compound for various industrial and medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1239450-42-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,4,5 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1239450-42:
(9*1)+(8*2)+(7*3)+(6*9)+(5*4)+(4*5)+(3*0)+(2*4)+(1*2)=150
150 % 10 = 0
So 1239450-42-0 is a valid CAS Registry Number.
1239450-42-0Relevant articles and documents
Efficient preparation of 2,4-methanoproline
Varnes, Jeffrey G.,Lehr, G. Scott,Moore, Gary L.,Hulsizer, James M.,Albert, Jeffrey S.
, p. 3756 - 3758 (2010)
Using a modification of the route described by Clardy and Hughes et al., 2,4-methanoproline hydrochloride (1) was prepared in four steps and 70% overall yield from DL-serine methyl ester.
Conversion of isomeric 2:3 adducts (aminoacid-formaldehyde) to N-acyl-pseudoprolines derivatives
Sélambarom, Jimmy,Smadja, Jacqueline,Pavia, André A.
, p. 615 - 617 (2007/10/03)
Reaction of acyl chlorides or acid anhydrides with isomeric 2:3 adducts derived from condensation of l-serine (1a), l-threonine (1b) and l-cysteine (1c) methyl esters with formaldehyde afforded N-acyl-pseudoprolines 7-19 in various yields. These 2:3 adducts can be considered as synthetic equivalents of oxaproline and thiaproline moieties. The present work revealed the versatile behaviour of the two 2:3 adducts as a consequence of the ring-chain tautomerism occurring in the five- and/or seven-membered rings.
