(R)-(-)-2-tert-Butylamino-1-phenylethanol

Base Information

Chemical Name:(R)-(-)-2-tert-Butylamino-1-phenylethanol
CAS No.:14467-51-7
Molecular Formula:C12H19 N O
Molecular Weight:177.28596
Hs Code.:2922199090
European Community (EC) Number:622-512-9
DSSTox Substance ID:DTXSID10537231
Nikkaji Number:J427.283H
Wikidata:Q82412172
Mol file:14467-51-7.mol

Synonyms:(R)-(-)-2-tert-Butylamino-1-phenylethanol;14467-51-7;(1R)-2-(TERT-BUTYLAMINO)-1-PHENYLETHANOL;(R)-(-)-2-TERT-BUTYLAMINO-1-PHENYLETHAN;(1R)-2-(tert-Butylamino)-1-phenylethan-1-ol;SCHEMBL421063;DTXSID10537231;(R)-(-)-2-tert-Butylamino-1-phenylethanol, 97%;J-007997

Suppliers and Price of (R)-(-)-2-tert-Butylamino-1-phenylethanol

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

Sigma-Aldrich
(R)-(?)-2-tert-Butylamino-1-phenylethanol 97%
1g
$ 134.00

American Custom Chemicals Corporation
(R)-(-)-2-TERT-BUTYLAMINO-1-PHENYLETHANOL 95.00%
5MG
$ 496.69

Total 4 raw suppliers

Chemical Property of (R)-(-)-2-tert-Butylamino-1-phenylethanol

Chemical Property:

Melting Point:105-108 °C(lit.)
Boiling Point:284°Cat760mmHg
Flash Point:80.7°C
PSA：32.26000
Density:0.989g/cm³
LogP:2.49900
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:193.146664230
Heavy Atom Count:14
Complexity:156

Purity/Quality:

97% ^*data from raw suppliers

(R)-(?)-2-tert-Butylamino-1-phenylethanol 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of (R)-(-)-2-tert-Butylamino-1-phenylethanol

There total 24 articles about (R)-(-)-2-tert-Butylamino-1-phenylethanol 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: 90.0%

: 21504-13-2
2.5-Dihydroxy-3.6-diphenyl-1.4-dioxan

: 75-64-9
tert-butylamine

: 14467-32-4,14467-51-7,18366-40-0,14467-31-3
2-(tert-butylamino)-1-phenylethan-1-ol

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; ethanol; for 0.5h;
DOI:10.3390/molecules171213864

Reference yield: 79.0%

: C₁₂H₁₅Cl₄NOSi

: 14467-51-7
(R)-1-Phenyl-2-(tert-butylamino)-1-ethanol

Guidance literature:: With ammonia borane; In diethyl ether; at -78 - 20 ℃; for 1h; enantioselective reaction; Inert atmosphere;
DOI:10.1002/chem.201500210