(r)-1-Methyl-3-phenylpiperazine

Base Information

Chemical Name:(r)-1-Methyl-3-phenylpiperazine
CAS No.:960403-87-6
Molecular Formula:C₁₁H₁₆N₂
Molecular Weight:176.261
Hs Code.:
UNII:754JEG656A
Wikidata:Q27896064

Synonyms:(r)-1-methyl-3-phenylpiperazine;(3R)-1-Methyl-3-phenylpiperazine;754JEG656A;1-Methyl-3-phenylpiperazine, (R)-;Piperazine, 1-methyl-3-phenyl-, (3R)-;UNII-754JEG656A;960403-87-6;SCHEMBL2910280;EN300-8127238;Q27896064

Suppliers and Price of (r)-1-Methyl-3-phenylpiperazine

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

Total 0 raw suppliers

Chemical Property of (r)-1-Methyl-3-phenylpiperazine

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:176.131348519
Heavy Atom Count:13
Complexity:152

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1CCNC(C1)C2=CC=CC=C2
Isomeric SMILES:CN1CCN[C@@H](C1)C2=CC=CC=C2

Technology Process of (r)-1-Methyl-3-phenylpiperazine

There total 7 articles about (r)-1-Methyl-3-phenylpiperazine 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: 87.0%

: 1074-12-0
phenylglyoxal hydrate

: 109-81-9
N-methyl-ethane-1,2-diamine

: 960403-87-6
(3R)-1-methyl-3-phenylpiperazine

Guidance literature:: With glucose-6-phosphate dehydrogenase; glucose-6-phosphate; Myxococcus stipitatus R-selective imine reductase; NADPH; magnesium chloride; In aq. phosphate buffer; at 25 ℃; for 4h; pH=7; enantioselective reaction; Enzymatic reaction;
DOI:10.1021/acscatal.8b00291

Reference yield: 52.0%

: 960403-87-6
(3R)-1-methyl-3-phenylpiperazine

: 1417826-88-0
(S)-1-(4-methyl-2-phenylpiperazin-1-yl)-3-phenylpropan-1-one

: (R)-1-(4-methyl-2-phenylpiperazin-1-yl)-3-phenylpropan-1-one

Guidance literature:: In dichloromethane; for 49h;

With triethylamine; In dichloromethane;

Reference yield: 27.0%

: C₁₅H₂₀O₂

: 5271-27-2
1-methyl-3-phenylpiperazine

: 960403-87-6
(3R)-1-methyl-3-phenylpiperazine

: 1346681-93-3
(2S)-1-(3-mesitylpropanoyl)-4-methyl-2-phenylpiperazine

: (2R)-1-(3-mesitylpropanoyl)-4-methyl-2-phenylpiperazine

Guidance literature:: With 2-(2,4,6-trimethyl-phenyl)-2,5,6,7-tetrahydro-pyrrolo[2,1-c] [1,2,4]triazol-4-ylium perchlorate; (4aR,9aS)-6-bromo-4-hydroxy-4,4a,9,9a-tetrahydroindeno[2,1-b][1,4]oxazin-3(2H)-one; potassium carbonate; In Isopropyl acetate; at 23 ℃; for 24h; Resolution of racemate;
DOI:10.1039/c2cc34907h