33492-83-0 Usage
Molecular structure
2,2,2-trichloroethyl (6R,7R)-3-(bromomethyl)-8-oxo-7-[(thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 5-oxide is a complex compound with a long molecular structure.
Functional groups
The compound contains trichloroethyl and bromomethyl groups, a thiophen-2-ylacetylamine group, a bicyclic structure with a thiazolidine ring, and a carboxylate group.
Stereochemistry
The compound has specific stereochemistry with 6R and 7R configurations.
Potential applications
Due to its unique structure and functional groups, this chemical may have various potential applications in the fields of chemistry, pharmacology, and biochemistry.
Further research
Understanding the specific properties and uses of this chemical would require additional research and investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 33492-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,9 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33492-83:
(7*3)+(6*3)+(5*4)+(4*9)+(3*2)+(2*8)+(1*3)=120
120 % 10 = 0
So 33492-83-0 is a valid CAS Registry Number.
33492-83-0Relevant articles and documents
Synthesis of 3-functionalised cephalosporins by photoinitiated bromination. Transformations of 2,2,2-trichloroethyl 1S, 6R, 7R)-3-bromomethyl-7-formamidoceph-3-EM-4-carboxylate, 1-oxide
Cowley,Humber,Laundon,et al.
, p. 461 - 467 (2007/10/02)
The 3-bromomethyl derivative 2c, obtained by photoinitiated bromination of the corresponding 3-Me compound 1c, has been converted into the antibiotics cephalothin 18 and cephaloridine 20. Reaction of 2c with lithium dimethyl- and diphenyl-cuprate led to the intermediates 22 and 24 respectively. Further transformation of 24 provided the 3-benzyl derivative 27, an isostere of cephaloridine.
