CID 11821248

Base Information

Chemical Name:CID 11821248
CAS No.:128593-67-9
Molecular Formula:C₁₈H₂₇N
Molecular Weight:257.419
Hs Code.:
DSSTox Substance ID:DTXSID901138681
Nikkaji Number:J998.721E

Synonyms:DTXSID901138681;128593-67-9;(1R,2R,4R)-1,7,7-Trimethyl-N-[(1R)-1-phenylethyl]bicyclo[2.2.1]heptan-2-amine

Suppliers and Price of CID 11821248

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of CID 11821248

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:257.214349865
Heavy Atom Count:19
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)NC2CC3CCC2(C3(C)C)C
Isomeric SMILES:C[C@H](C1=CC=CC=C1)N[C@@H]2C[C@H]3CC[C@@]2(C3(C)C)C

Technology Process of CID 11821248

There total 3 articles about CID 11821248 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: 62.0%

: 97505-89-0,125346-70-5
(R)-N-(1-phenylethyl)bornanimine

: 128593-67-9,128593-69-1
exo-(1R)-N-(1-phenylethyl)bornanamine

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In methanol; for 48h; Ambient temperature;
DOI:10.1016/S0040-4020(01)85435-1

Reference yield:

: 736109-58-3,787517-91-3,68546-28-1
1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one

: 128593-67-9,128593-69-1
exo-(1R)-N-(1-phenylethyl)bornanamine

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / camphorsulphonic acid, molecular sieve / 120 h / 120 °C

2: 62 percent / 1.) methanolic HCl, 2.) NaBH₃CN / methanol / 48 h / Ambient temperature

With hydrogenchloride; molecular sieve; camphor-10-sulfonic acid; sodium cyanoborohydride; In methanol;
DOI:10.1016/S0040-4020(01)85435-1

Reference yield:

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 128593-67-9,128593-69-1
exo-(1R)-N-(1-phenylethyl)bornanamine

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / camphorsulphonic acid, molecular sieve / 120 h / 120 °C

2: 62 percent / 1.) methanolic HCl, 2.) NaBH₃CN / methanol / 48 h / Ambient temperature

With hydrogenchloride; molecular sieve; camphor-10-sulfonic acid; sodium cyanoborohydride; In methanol;
DOI:10.1016/S0040-4020(01)85435-1