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(1S,5R)-3-benzyl-6-(2-bromo-1-hydroxy-2-methylpropyl)-4-oxa-2,6-diazabicyclo[3.2.0]hept-2-en-7-one is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1S,5R configuration indicating the arrangement of atoms in space. The compound features a benzyl group attached to the 3-position, a 2-bromo-1-hydroxy-2-methylpropyl group at the 6-position, and a 4-oxa-2,6-diazabicyclo[3.2.0]hept-2-en-7-one core structure. This core structure consists of a seven-membered ring with two nitrogen atoms, one oxygen atom, and a double bond, which contributes to the molecule's reactivity and potential applications in various chemical and pharmaceutical contexts. The presence of a bromine atom and a hydroxyl group suggests that (1S,5R)-3-benzyl-6-(2-bromo-1-hydroxy-2-methylpropyl)-4-oxa-2,6-diazabicyclo<3.2.0>hept-2-en-7-one may have interesting properties in terms of reactivity and solubility, and it could be a candidate for further study in the development of new drugs or other chemical products.

74213-36-8

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74213-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74213-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,1 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74213-36:
(7*7)+(6*4)+(5*2)+(4*1)+(3*3)+(2*3)+(1*6)=108
108 % 10 = 8
So 74213-36-8 is a valid CAS Registry Number.

74213-36-8Relevant academic research and scientific papers

STUDIES RELATED TO PENICILLINS. PART 23. PREPARATION OF THE N-PHENYLACETYL AND N-TRIPHENYLMETHYL DERIVATIVES OF (3R,4R)-3-AMINO-4-t-BUTHYLTHIOAZETIDIN-2-ONE

Corbett, David F.,Kaura, Arun C.,Maycock, Christopher D.,Stoodley, Richard J.

, p. 2009 - 2016 (2007/10/02)

Addition of hypobromous acid to the alkene moiety of the 6-substituent of (1S,5R)-3-benzyl-6-(2-methylprop-1-enyl)-4-oxa-2,6-diazabicyclohept-2-en-7-one (7a) was effected by the action of N-bromoacetamide in aqueous acetone.On the basis of 1H NMR s

(3R,4R)-4-t-Butylthio-3-phenylacetamidoazetidin-2-one: a Useful Precursor of Penicillin Analogues

Kaura, Arun C.,Maycock, Christopher D.,Stoodley, Richard J.

, p. 34 - 35 (2007/10/02)

The preparation of the title azetidinone and its conversion into (1S,5R,6R)-2,2-dimethyl-6-phenylacetamidopenam 1-oxide are described.

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