N-[(1R)-1-phenylethyl]benzamide

Base Information

Chemical Name:N-[(1R)-1-phenylethyl]benzamide
CAS No.:20826-48-6
Molecular Formula:C15H15 N O
Molecular Weight:225.29
Hs Code.:2924299090
DSSTox Substance ID:DTXSID70350206
Nikkaji Number:J1.284.963J
Wikidata:Q82126021
Mol file:20826-48-6.mol

Synonyms:N-[(1R)-1-phenylethyl]benzamide;20826-48-6;(R)-N-(1-Phenylethyl)benzamide;(R)-(+)-N-BENZOYL-a-METHYLBENZYLAMINE;N-(1-Phenyl-ethyl)-benzamide;SCHEMBL5968858;DTXSID70350206;AKOS004909389;Z1147902969

Suppliers and Price of N-[(1R)-1-phenylethyl]benzamide

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
Packaging
price

American Custom Chemicals Corporation
(R)-(+)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE 95.00%
5MG
$ 505.69

Total 6 raw suppliers

Chemical Property of N-[(1R)-1-phenylethyl]benzamide

Chemical Property:

Vapor Pressure:2.34E-07mmHg at 25°C
Melting Point:123-125oC
Boiling Point:422.8°C at 760 mmHg
Flash Point:254.9°C
PSA：32.59000
Density:1.084g/cm³
LogP:3.75240
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:225.115364102
Heavy Atom Count:17
Complexity:239

Purity/Quality:

99% ^*data from raw suppliers

(R)-(+)-N-BENZOYL-ALPHA-METHYLBENZYLAMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1=CC=CC=C1)NC(=O)C2=CC=CC=C2
Isomeric SMILES:C[C@H](C1=CC=CC=C1)NC(=O)C2=CC=CC=C2

Technology Process of N-[(1R)-1-phenylethyl]benzamide

There total 153 articles about N-[(1R)-1-phenylethyl]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: 98.0%

: 93-58-3,5705-52-2,80226-58-0
benzoic acid methyl ester

: 2627-86-3
(S)-1-phenyl-ethylamine

: 3480-59-9,4108-58-1,20826-48-6,28623-68-9
(S)-N-(1-phenylethyl)benzamide

Guidance literature:: With gallium; iodobenzene; aluminium; at 120 ℃; for 20h; Inert atmosphere;

(S)-1-phenyl-ethylamine; In toluene; at 20 ℃; for 0.166667h;

benzoic acid methyl ester; In touene; at 80 ℃; for 3h;
DOI:10.1055/s-0029-1219179

Reference yield: 94.0%

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

: 611-74-5
N,N-dimethylbenzamide

: 20826-48-6
(R)-N-(1-phenylethyl)benzamide

Guidance literature:: With Imidazole hydrochloride; at 150 ℃; for 3h; Sealed tube;
DOI:10.3390/molecules23092234

Reference yield: 93.0%

: 17279-30-0
(S)-(-)-α-methylbenzylamine hydrochloride

: 100-51-6,185532-71-2
benzyl alcohol

: 3480-59-9,4108-58-1,20826-48-6,28623-68-9
(S)-N-(1-phenylethyl)benzamide

Guidance literature:: With tert.-butylhydroperoxide; calcium carbonate; sodium iodide; In water; acetonitrile; at 80 ℃; for 4h; Inert atmosphere; Green chemistry;
DOI:10.1016/j.tetlet.2014.07.085