(R)-1-Azido-3-phenyl-2-propanol

Base Information

Chemical Name:(R)-1-Azido-3-phenyl-2-propanol
CAS No.:112009-62-8
Molecular Formula:C9H11N3O
Molecular Weight:177.20300
Hs Code.:
DSSTox Substance ID:DTXSID501295811
Nikkaji Number:J940.097D
Mol file:112009-62-8.mol

Synonyms:(2R)-1-azido-3-phenylpropan-2-ol;112009-62-8;(R)-1-Azido-3-phenyl-2-propanol;DTXSID501295811;(alphaR)-alpha-(Azidomethyl)benzeneethanol;EN300-211586

Suppliers and Price of (R)-1-Azido-3-phenyl-2-propanol

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

TRC
(2R)-1-Azido-3-phenylpropan-2-ol
100mg
$ 285.00

TRC
(2R)-1-Azido-3-phenylpropan-2-ol
50mg
$ 200.00

TRC
(2R)-1-Azido-3-phenylpropan-2-ol
10mg
$ 45.00

AK Scientific
(R)-1-Azido-3-phenyl-2-propanol
10g
$ 3412.00

AK Scientific
(R)-1-Azido-3-phenyl-2-propanol
5g
$ 2332.00

Total 1 raw suppliers

Chemical Property of (R)-1-Azido-3-phenyl-2-propanol

Chemical Property:

PSA：69.98000
LogP:1.35306
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:177.090211983
Heavy Atom Count:13
Complexity:183

Purity/Quality:: (2R)-1-Azido-3-phenylpropan-2-ol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(CN=[N+]=[N-])O
Isomeric SMILES:C1=CC=C(C=C1)C[C@H](CN=[N+]=[N-])O

Technology Process of (R)-1-Azido-3-phenyl-2-propanol

There total 5 articles about (R)-1-Azido-3-phenyl-2-propanol 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: 93.0%

: 112009-61-7
(R)-1-chloro-2-hydroxy-3-phenylpropane

: 112009-62-8
(R)-1-azido-3-phenylpropan-2-ol

Guidance literature:: With sodium azide; In N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)95420-0

Reference yield: 88.0%

: 17131-14-5,19881-97-1,61475-32-9,79299-22-2
(R)-3-phenylpropane-1,2-diol

: 112009-62-8
(R)-1-azido-3-phenylpropan-2-ol

Guidance literature:: (R)-3-phenylpropane-1,2-diol; With di(n-butyl)tin oxide; triethylamine; p-toluenesulfonyl chloride; In dichloromethane; at 0 - 20 ℃;

With sodium azide; In N,N-dimethyl-formamide; at 70 ℃; for 10h; regioselective reaction;
DOI:10.1016/j.tet.2010.01.047

Reference yield:

: 4436-24-2
1,2-epoxy-3-phenylpropane

: C₉H₁₁N₃O

: 61393-94-0
(R)-2-benzyloxirane

: 112009-62-8
(R)-1-azido-3-phenylpropan-2-ol

: 91420-74-5
(S)-(2,3-epoxypropyl)benzene

Guidance literature:: With sodium azide; sulfuric acid; Halohydrin dehalogenase from Arthrobacter sp. AD₂, N₁₇₈A mutant; 2-amino-2-hydroxymethyl-1,3-propanediol; In water; dimethyl sulfoxide; at 20 ℃; pH=7.0; Reagent/catalyst; enantioselective reaction; Catalytic behavior; Resolution of racemate; Enzymatic reaction;
DOI:10.1016/j.tetasy.2016.08.003