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((2S,3R)-2-Benzo[1,3]dioxol-5-yl-4-oxo-3-phenoxy-azetidin-1-yl)-acetic acid is a complex organic compound with a molecular formula of C18H15NO6. It features a 4-oxo-azetidin-1-yl core, which is a cyclic amine with a four-membered ring, and is substituted with a benzo[1,3]dioxol-5-yl group at the 2-position and a phenoxy group at the 3-position. The molecule also contains a carboxylic acid group at the end of the acetic acid chain. ((2S,3R)-2-Benzo[1,3]dioxol-5-yl-4-oxo-3-phenoxy-azetidin-1-yl)-acetic acid is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the muscarinic acetylcholine receptors, which are involved in various physiological processes. Its chiral centers at the 2 and 3 positions give rise to stereoisomers, with the specific (2S,3R) configuration being of interest for its biological activity.

76640-35-2

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76640-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76640-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76640-35:
(7*7)+(6*6)+(5*6)+(4*4)+(3*0)+(2*3)+(1*5)=142
142 % 10 = 2
So 76640-35-2 is a valid CAS Registry Number.

76640-35-2Relevant academic research and scientific papers

Studies on β-Lactams: Synthesis of Some Steroid-type Di-β-lactams

Sharma, S. D.,Gupta, Sangita,Mehra, Usha

, p. 204 - 207 (2007/10/02)

Schiff bases (1) on reaction with phenoxyacetyl chloride yield the β-lactam esters (2) which on further hydrolysis under mild basic conditions afford α-(2-oxo-1-azetidino)acetic acids (3).Reaction of the imines (4) with 3 using POCl3 and triethylamine fur

Conversion of some monocyclic β-lactams into novel di-β-lactams

Sharma,Gupta,Bindra,Sunita

, p. 3295 - 3298 (2007/10/02)

Monocyclic β-lactams (V & XI) carrying a carboxy function have been used to annelate the Schiff bases (II & X) using POCl3 in the presence of triethylamine to obtain the di-β-lactams (VI & XII). Alternately, (VI) could also be prepared by annelation of the Schiff base (IX) derived from the α-amino-β-lactam (VIII), with phenoxyacetyl chloride.

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