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"6α-hydroxy-6β-phenyl-8-(2-phenylethyl)-8-azabicyclo<3.2.1>octane" is a complex organic compound with a unique molecular structure. It features a bicyclic ring system with a nitrogen atom incorporated into the ring, making it an azabicycle. The compound has a hydroxyl group at the 6α position and a phenyl group at the 6β position, which are both attached to the same carbon atom. Additionally, it has a 2-phenylethyl substituent at the 8 position, further enhancing its structural complexity. This chemical is characterized by its specific arrangement of functional groups and aromatic rings, which contribute to its potential applications in various fields, such as pharmaceuticals or chemical research.

101006-66-0

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101006-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101006-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101006-66:
(8*1)+(7*0)+(6*1)+(5*0)+(4*0)+(3*6)+(2*6)+(1*6)=50
50 % 10 = 0
So 101006-66-0 is a valid CAS Registry Number.

101006-66-0Relevant academic research and scientific papers

Novel 6-substituted 8-azabicyclo [3.2.1.] octanes as potential opiate agonists and antagonists

Dewar,Parfitt,Sheh

, p. 228 - 234 (2007/10/02)

Reaction of 8-methyl-8-azabicyclo[3.2.1]octan-6-one (tropan-6-one) with aryl magnesium halides selectively yields 6β-aryl-6α-hydroxy-8-methyl-8-azabicyclo[3.2.1]octanes (6β-aryl-6α-hydroxytropanes). 1H nmr studies supporting the assignment are presented, together with 13C data of these alcohols and various derivatives prepared as potential agonists and antagonists of opiate receptors. The results from 1H nmr studies of 6-hydroxytropan-3-one, the synthesis of which was reported in 1952, support the assigned 6β-hydroxy stereochemistry.

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