(3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate

Base Information

Chemical Name:(3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate
CAS No.:3818-30-2
Molecular Formula:C₁₇H₂₃NO₂
Molecular Weight:273.375
Hs Code.:
DSSTox Substance ID:DTXSID101159401
Nikkaji Number:J506.262D,J588.407A,J588.408J

Synonyms:SCHEMBL23494998;SCHEMBL23494999;DTXSID101159401;(3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate;2-Phenylpropanoic acid (1beta,5beta)-8-methyl-8-azabicyclo[3.2.1]octan-3alpha-yl ester;(R)-alpha-Methylbenzeneacetic acid (1beta,5beta)-8-methyl-8-azabicyclo[3.2.1]octan-3alpha-yl ester;(S)-alpha-Methylbenzeneacetic acid (1beta,5beta)-8-methyl-8-azabicyclo[3.2.1]octan-3alpha-yl ester;3818-30-2

Suppliers and Price of (3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of (3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:273.172878976
Heavy Atom Count:20
Complexity:337

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)C(=O)OC2CC3CCC(C2)N3C
Isomeric SMILES:CC(C1=CC=CC=C1)C(=O)OC2C[C@H]3CC[C@@H](C2)N3C

Technology Process of (3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate

There total 1 articles about (3-endo)-8-Methyl-8-azabicyclo[3.2.1]oct-3-yl alpha-methylbenzeneacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%