(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine

Base Information Edit

Chemical Name:(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine
CAS No.:70749-06-3
Molecular Formula:C₁₆H₂₀N₂
Molecular Weight:240.348
Hs Code.:29215990
European Community (EC) Number:684-729-5,695-310-1
DSSTox Substance ID:DTXSID40427111
Wikidata:Q72469893
Mol file:70749-06-3.mol

Synonyms:70749-06-3;60508-97-6;(1S,2S)-N,N'-Dimethyl-1,2-diphenylethane-1,2-diamine;(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine;(1S,2S)-(-)-N,N'-DIMETHYL-1,2-DIPHENYL-1,2-ETHANE DIAMINE;(1S,2S)-N,N'-Dimethyl-1,2-diphenylethylenediamine;ST50405145;SCHEMBL8147964;DTXSID40427111;1,2-Ethanediamine, N,N'-dimethyl-1,2-diphenyl-, (1S,2S)-;MFCD00216956;AKOS015899566;BS-51458;CS-0098018;E76546;(1S,2S)-(-)-N,N'-Dimethyl-1,2-diphenylethylenediamine;(1S,2S)-N,N'-Dimethyl-1,2-diphenyl-1,2-ethanediamine;1,2-Ethanediamine,N,N'-dimethyl-1,2-diphenyl-,(1S,2S)-;rel-(1S,2S)-N,N'-Dimethyl-1,2-diphenylethane-1,2-diamine;(1S,2S)-N,N'-Dimethyl-1,2-diphenyl-1,2-ethylenediamine, 97%

Suppliers and Price of (1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine

Supply Marketing:Edit

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

Sigma-Aldrich
(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine 97%
100mg
$ 95.70

Crysdot
(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine 95+%
25g
$ 2232.00

Crysdot
(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine 95+%
10g
$ 1092.00

Crysdot
(1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine 95+%
5g
$ 713.00

Chemenu
(1S,2S)-N,N''-Dimethyl-1,2-diphenyl-1,2-ethanediamine 95%+
1g
$ 736.00

Chemenu
(1S,2S)-N,N''-Dimethyl-1,2-diphenyl-1,2-ethanediamine 95%+
100mg
$ 86.00

Biosynth Carbosynth
(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine
10 mg
$ 50.00

Biosynth Carbosynth
(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine
50 mg
$ 160.00

Biosynth Carbosynth
(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine
25 mg
$ 100.00

Biosynth Carbosynth
(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine
250 mg
$ 450.00

Total 14 raw suppliers

Chemical Property of (1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine Edit

Chemical Property:

Appearance/Colour:white to light yellow crystals or crystalline powder
Melting Point:48-51 °C
Refractive Index:1.5519 (estimate)
Boiling Point:346.4 °C at 760 mmHg
PKA:9.14±0.30(Predicted)
Flash Point:193.9 °C
PSA：24.06000
Density:1.0485 (rough estimate)
LogP:3.68960
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:240.162648646
Heavy Atom Count:18
Complexity:193

Purity/Quality:

98%min ^*data from raw suppliers

(1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s): C
Hazard Codes:C,N,Xn
Statements: 34-50-22
Safety Statements: 45-36/37/39-26-61

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(C1=CC=CC=C1)C(C2=CC=CC=C2)NC
Isomeric SMILES:CN[C@@H](C1=CC=CC=C1)[C@H](C2=CC=CC=C2)NC
Uses (1S,2S)-N,N′-Dimethyl-1,2-diphenyl-1,2-ethylenediamine can be used as:A precursor for the synthesis of chiral imidazolinium salts, which are used as catalysts for aza Diels?Alder reaction and as shift reagents for potassium salt of Mosher′s acid.A ligand in the preparation of 2,3-dihydrobenzofurans and indanes by reacting alkyl halides with alkyl electrophiles using nickel/diamine catalyst.A ligand in the synthesis of carbamates, sulfonamides, and sulfones through alkyl-alkyl Suzuki reaction using Ni catalyst.

Technology Process of (1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine

There total 23 articles about (1S,2S)-N1,N2-Dimethyl-1,2-diphenylethane-1,2-diamine 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%