3-phenyl-3,4-dihydro-2H-1,4-benzoxazine

Base Information

Chemical Name:3-phenyl-3,4-dihydro-2H-1,4-benzoxazine
CAS No.:70310-30-4
Molecular Formula:C14H13NO
Molecular Weight:211.263
Hs Code.:
European Community (EC) Number:871-037-5
DSSTox Substance ID:DTXSID20499654
Nikkaji Number:J2.001.067C
Mol file:70310-30-4.mol

Synonyms:70310-30-4;3-phenyl-3,4-dihydro-2H-1,4-benzoxazine;3-phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine;SCHEMBL5451243;DTXSID20499654;BKQRBYFLQYHTCV-UHFFFAOYSA-N;AKOS022961309;CS-0455087;3-phenyl-3,4-dihydro-2H-benzo[1,4]oxazine;EN300-265431;F92000;F1907-0419

Suppliers and Price of 3-phenyl-3,4-dihydro-2H-1,4-benzoxazine

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

Crysdot
3-Phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine 97%
10g
$ 1736.00

Crysdot
3-Phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine 97%
5g
$ 1240.00

Crysdot
3-Phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine 97%
1g
$ 446.00

AK Scientific
3-Phenyl-3,4-dihydro-2H-1,4-benzoxazine
100mg
$ 262.00

Total 5 raw suppliers

Chemical Property of 3-phenyl-3,4-dihydro-2H-1,4-benzoxazine

Chemical Property:

PSA：21.26000
LogP:3.37020
XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:211.099714038
Heavy Atom Count:16
Complexity:225

Purity/Quality:

97% ^*data from raw suppliers

3-Phenyl-3,4-dihydro-2H-benzo[b][1,4]oxazine 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(NC2=CC=CC=C2O1)C3=CC=CC=C3

Technology Process of 3-phenyl-3,4-dihydro-2H-1,4-benzoxazine

There total 17 articles about 3-phenyl-3,4-dihydro-2H-1,4-benzoxazine 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: 100.0%

: 18065-01-5
2-(2-nitrophenoxy)-1-phenyl-1-ethanone

: 70310-30-4
3,4-dihydro-3-phenyl-2H-1,4-benzoxazine

Guidance literature:: With sodium hypophosphite; palladium 10% on activated carbon; In tetrahydrofuran; water; at 20 ℃; for 36h;

Reference yield: 99.0%

: 70310-30-4
3,4-dihydro-3-phenyl-2H-1,4-benzoxazine

Guidance literature:: With hydrogen; C₄₀H₃₆FeN₂P₂; at 20 ℃; for 24h; under 45004.5 Torr; Inert atmosphere;

Reference yield: 98.0%

: 19409-26-8
3-phenyl-2H-1,4-benzoxazine

: 70310-30-4
3,4-dihydro-3-phenyl-2H-1,4-benzoxazine

Guidance literature:: With thiourea S,S-dioxide; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; In chloroform; at 60 ℃; for 16h;
DOI:10.1007/s10562-017-2061-1