Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-

Base Information

Chemical Name:Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-
CAS No.:1322805-22-0
Molecular Formula:C₁₄H₁₉NO₂
Molecular Weight:233.31
Hs Code.:
DSSTox Substance ID:DTXSID401164718

Synonyms:DTXSID401164718;Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-;1322805-22-0

Suppliers and Price of Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-

Supply Marketing:

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

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Chemical Property of Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:233.141578849
Heavy Atom Count:17
Complexity:255

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COCCC(=O)NC1CCC2=CC=CC=C2C1
Isomeric SMILES:COCCC(=O)N[C@@H]1CCC2=CC=CC=C2C1

Technology Process of Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]-

There total 1 articles about Propanamide, 3-methoxy-N-[(2R)-1,2,3,4-tetrahydro-2-naphthalenyl]- 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:

: 2954-50-9
2-aminotetralin

: 3852-09-3
methyl 3-methoxypropionate

: 1322805-22-0
(R)-N-(1,2,3,4-tetrahydronaphthalen-3-yl)-3-methoxypropanamide

: 2217-42-7,2954-50-9,21880-87-5,21966-60-9
(2R)-2-amino-1,2,3,4-tetrahydronaphthalene

: 2217-42-7,2954-50-9,21880-87-5,21966-60-9
(2S)-(1,2,3,4-tetrahydronaphthalen-2-yl)amine

Guidance literature:: With supported Candida antartica lipase B; In tert-butyl methyl ether; at 38 - 40 ℃; for 20h; optical yield given as %ee; enantioselective reaction; Molecular sieve; Enzymatic reaction;
DOI:10.1021/jo201256w