(1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol

Base Information

Chemical Name:(1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol
CAS No.:49801-14-1
Molecular Formula:C12H12 O2
Molecular Weight:188.226
Hs Code.:2906299090
DSSTox Substance ID:DTXSID20452542
Nikkaji Number:J723.204G
Wikidata:Q27454946
Mol file:49801-14-1.mol

Synonyms:(1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol;49801-14-1;(1R)-1-naphthalen-2-ylethane-1,2-diol;(R)-1-(2-naphthyl)-1,2-ethanediol;(R)-1-(Naphthalen-2-yl)ethane-1,2-diol;SCHEMBL6543395;DTXSID20452542;AKOS015913294;CS-0263757;EN300-8981439;(R)-(-)-1-(2-Naphthyl)-1,2-ethanediol, 98%;Q27454946;4T7

Suppliers and Price of (1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol

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)-(-)-1-(2-NAPHTHYL)-1,2-ETHANEDIOL 95.00%
5MG
$ 502.36

Total 6 raw suppliers

Chemical Property of (1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:131-135 °C(lit.)
Refractive Index:1.668
Boiling Point:402.3°Cat760mmHg
Flash Point:202.3°C
PSA：40.46000
Density:1.237g/cm³
LogP:1.86550
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:188.083729621
Heavy Atom Count:14
Complexity:181

Purity/Quality:

98% ^*data from raw suppliers

(R)-(-)-1-(2-NAPHTHYL)-1,2-ETHANEDIOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)C(CO)O
Isomeric SMILES:C1=CC=C2C=C(C=CC2=C1)[C@H](CO)O

Technology Process of (1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol

There total 4 articles about (1r)-1-(Naphthalen-2-Yl)ethane-1,2-Diol 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: 76.0%

: 43210-74-8,49801-14-1,13603-65-1
(+/-)-1-(2-naphthalenyl)-ethane-1,2-diol

: 93-09-4
naphthalene-2-carboxylate

Guidance literature:: Conversion of starting material;

Reference yield: 50.0%

: 86457-71-8,146145-08-6,20861-99-8
2-(naphthalen-2-yl)oxirane

: 43210-74-8,49801-14-1,13603-65-1
(+/-)-1-(2-naphthalenyl)-ethane-1,2-diol

: 93-09-4
naphthalene-2-carboxylate

Guidance literature:: With oxygen; bismuth mandelate; In dimethyl sulfoxide; at 80 ℃; for 2.3h; under 760 Torr;
DOI:10.1016/0022-328X(94)88192-8

Reference yield:

: 43210-74-8,49801-14-1,13603-65-1
(+/-)-1-(2-naphthalenyl)-ethane-1,2-diol

: 98-88-4
benzoyl chloride

: 49801-14-1
(S)-1-(2-naphthyl)-1,2-ethanediol

: 43210-74-8
(S)-1-(naphthalen-2-yl)-1,2-ethanediol

: 2-hydroxy-2-(naphthalen-2-yl)ethyl benzoate

: (R)-2-hydroxy-2-(naphthalen-2-yl)ethyl benzoate

Guidance literature:: With sodium carbonate; (S)-4,4-Br₂-4,5-dihydro-3H-dinaphtho[2,1-c:1',2'-e]stannepin; In tetrahydrofuran; water; at -10 ℃; for 17h; Title compound not separated from byproducts.;
DOI:10.1021/ol9908373