168133-91-3 Usage
Chemical structure
A unique structure with a spiro central ring system and a phenylmethyl group.
Classification
Belongs to the class of spirolactams, which are heterocyclic compounds.
Functional groups
Contains a carbonyl group (C=O) and a phenylmethyl group (C6H5-CH2-).
Potential reactivity
The presence of the phenylmethyl group adds to the molecule's complexity and may influence its reactivity.
Applications
May have uses in the pharmaceutical and agrochemical industries, as well as in organic synthesis and chemical research.
Further exploration
More research is needed to fully understand its capabilities and implications in various fields.
Please note that the provided material does not include specific details about the compound's properties, such as molecular weight, solubility, or stability. Further research and analysis would be required to obtain this information.
Check Digit Verification of cas no
The CAS Registry Mumber 168133-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,1,3 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 168133-91:
(8*1)+(7*6)+(6*8)+(5*1)+(4*3)+(3*3)+(2*9)+(1*1)=143
143 % 10 = 3
So 168133-91-3 is a valid CAS Registry Number.
168133-91-3Relevant articles and documents
Cyclization via carbolithiation of α-amino alkyllithium reagents
Bahde, Robert J.,Rychnovsky, Scott D.
supporting information; experimental part, p. 4017 - 4020 (2009/06/18)
(Chemical Equation Presented) We report a new route to tertiary α-amino stereocenters by sequential alkylation of α-amino nitriles followed by reductive lithiation of the nitrile and cycllzation onto an alkene. Reductive lithiation of α-amino nitriles usi
FORMAL SYNTHESIS OF (+/-)-PERHYDROHISTRIONICOTOXIN
Holmes, Andrew B.,Russell, Keith,Stern, Edward S.,Stubbs, Michael E.,Wellard, Nicolas K.
, p. 4163 - 4166 (2007/10/02)
The syntheses of 1-benzyl-7-butyl-1-azaspirocycloundec-7-ene (14) a formal precursor of perhydrohistrionicotoxin (2) and the thermodynamically preferred exocyclic isomer (13) in six steps from the readily available N-benzyloxycarbonyl-10-amino-Δsup
