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(2S,5R)-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-, DIPHENYLMETHYL ESTER, 4-OXIDE is a complex organic compound featuring a bicyclic ring system with a thiolactam ring, a carboxylic acid group, and a diphenylmethyl ester group. The 7-oxo and 4-oxide substitutions contribute to its unique chemical properties. Derived from the parent compound 4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, its specific characteristics, applications, and uses are determined by its structural and functional attributes.

76911-24-5

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76911-24-5 Usage

Uses

As the provided materials do not specify any particular uses for (2S,5R)-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID, 3,3-DIMETHYL-7-OXO-, DIPHENYLMETHYL ESTER, 4-OXIDE, it is not possible to list its applications based on the information given. However, given its complex structure, it may have potential uses in various fields such as pharmaceuticals, materials science, or as an intermediate in chemical synthesis, depending on its reactivity, stability, and other properties. Further research and experimentation would be required to determine its practical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76911-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,1 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76911-24:
(7*7)+(6*6)+(5*9)+(4*1)+(3*1)+(2*2)+(1*4)=145
145 % 10 = 5
So 76911-24-5 is a valid CAS Registry Number.

76911-24-5Downstream Products

76911-24-5Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF 6α-HALOPENICILLANATES BY SAMARIUM(II) IODIDE PROMOTED REDUCTION OF 6,6-DIHALOPENICILLANATES

Kang, Han-Young,Pae, Ae Nim,Cho, Yong Seo,Choi, Kyung Il,Koh, Hun Yeong,Chung, Bong Young

, p. 2337 - 2342 (2007/10/03)

A mild an efficient samarium(II) iodide promoted-reduction of 6,6-dibromopenicillanates for stereoselective synthesis of 6α-bromopenicillanates has been developed.

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