N-(1-Naphthylmethyl)benzamide

Base Information

Chemical Name:N-(1-Naphthylmethyl)benzamide
CAS No.:32280-54-9
Molecular Formula:C₁₈H₁₅NO
Molecular Weight:261.323
Hs Code.:
DSSTox Substance ID:DTXSID801299874
Nikkaji Number:J1.084.989F

Synonyms:N-(1-Naphthylmethyl)benzamide;SCHEMBL3817884;N-(1-Naphthalenylmethyl)benzamide;DTXSID801299874;32280-54-9

Suppliers and Price of N-(1-Naphthylmethyl)benzamide

Supply Marketing:

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

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Chemical Property of N-(1-Naphthylmethyl)benzamide

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:261.115364102
Heavy Atom Count:20
Complexity:321

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NCC2=CC=CC3=CC=CC=C32

Technology Process of N-(1-Naphthylmethyl)benzamide

There total 12 articles about N-(1-Naphthylmethyl)benzamide 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: 88.0%

: potassium N-(trifluoroboratomethyl)benzamide

: 38262-42-9
1-naphthyl mesylate

: 32280-54-9
N-(naphthalen-1-ylmethyl)benzamide

Guidance literature:: With potassium phosphate; palladium diacetate; XPhos; In water; tert-butyl alcohol; at 110 ℃; for 4h; Inert atmosphere; Sealed tube;
DOI:10.1021/ol200128y

Reference yield: 82.0%

: 4780-79-4
1-naphthalene methanol

: 932-90-1
Benzaldoxime

: 32280-54-9
N-(naphthalen-1-ylmethyl)benzamide

Guidance literature:: Benzaldoxime; With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; In toluene; at 130 ℃; for 3h; Inert atmosphere; Schlenk technique; Green chemistry;

1-naphthalene methanol; With caesium carbonate; In toluene; at 130 ℃; for 12h; Inert atmosphere; Schlenk technique; Green chemistry;
DOI:10.1002/cctc.201300140

Reference yield: 80.0%

: 118-31-0
(naphth-1-yl)methylamine

: 7338-94-5
1,3-diphenyl-2-propynone

: 32280-54-9
N-(naphthalen-1-ylmethyl)benzamide

Guidance literature:: (naphth-1-yl)methylamine; 1,3-diphenyl-2-propynone; With lithium tert-butoxide; In dichloromethane; at 20 ℃; for 0.0833333h;

In dichloromethane; at 20 ℃; chemoselective reaction;
DOI:10.1039/c7cc09310a