2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one

Base Information

Chemical Name:2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one
CAS No.:10514-70-2
Molecular Formula:C10H11NO2
Molecular Weight:177.203
Hs Code.:
European Community (EC) Number:818-542-9
DSSTox Substance ID:DTXSID90442374
Nikkaji Number:J2.816.751B
Wikidata:Q82259615
ChEMBL ID:CHEMBL2407991
Mol file:10514-70-2.mol

Synonyms:10514-70-2;2,2-DIMETHYL-2H-BENZO[B][1,4]OXAZIN-3(4H)-ONE;2,2-dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one;2,2-DIMETHYL-4H-1,4-BENZOXAZIN-3-ONE;MFCD11868710;CHEMBL2407991;2H-1,4-Benzoxazin-3(4H)-one, 2,2-dimethyl-;SCHEMBL1450379;DTXSID90442374;LJRUKUQEIHJTEL-UHFFFAOYSA-N;BDBM50438256;2,2-Dimethyl-1,4-benzoxazin-3-one;AKOS006342025;AB64917;AS-65484;SY130765;2,2-dimethyl-4H-benzo[1,4]oxazin-3-one;CS-0061088;EN300-112429;2,2-DIMETHYL-2H-1,4-BENZOXAZIN-3(4H)-ONE;2,2-Dimethyl-2,3-dihydro-4H-1,4-benzooxazine-3-one;Z1203162506;2,2-Dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one, AldrichCPR

Suppliers and Price of 2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one

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
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price

Total 9 raw suppliers

Chemical Property of 2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:177.078978594
Heavy Atom Count:13
Complexity:225

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C(=O)NC2=CC=CC=C2O1)C

Technology Process of 2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one

There total 14 articles about 2,2-Dimethyl-2H-benzo[B][1,4]oxazin-3(4H)-one 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: 94.0%

: 600-00-0
ethyl 2-bromoisobutyrate

: 95-55-6
2-amino-phenol

: 10514-70-2
2,2-dimethyl-2H-1,4-benzoxazine-3-one

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-octyl-3-methylimidazolium tetrafluoroborate; at 20 ℃; for 2h; chemoselective reaction;
DOI:10.1016/j.tetlet.2010.01.122