2,1-Benzisoxazole, 3,7-dimethyl-

Base Information

Chemical Name:2,1-Benzisoxazole, 3,7-dimethyl-
CAS No.:38962-91-3
Molecular Formula:C₉H₉NO
Molecular Weight:147.177
Hs Code.:
DSSTox Substance ID:DTXSID20192254
Wikidata:Q83064910
Mol file:38962-91-3.mol

Synonyms:2,1-Benzisoxazole, 3,7-dimethyl-;3,7-Dimethyl-2,1-benzisoxazole;38962-91-3;SCHEMBL8404505;DTXSID20192254

Suppliers and Price of 2,1-Benzisoxazole, 3,7-dimethyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 2,1-Benzisoxazole, 3,7-dimethyl-

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:147.068413911
Heavy Atom Count:11
Complexity:149

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC2=C(ON=C12)C

Technology Process of 2,1-Benzisoxazole, 3,7-dimethyl-

There total 2 articles about 2,1-Benzisoxazole, 3,7-dimethyl- 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:

: 102878-74-0
2-methyl-6-ethylnitrobenzene

: 38962-91-3
3,7-dimethyl-2,1-benzisoxazole

: 102878-76-2
3-ethyl-6-nitrotoluene

: 102878-75-1
2-Ethyl-4-methylnitrobenzene

Guidance literature:: With trifluorormethanesulfonic acid; at 110 ℃;

Reference yield:

: 102878-74-0
2-methyl-6-ethylnitrobenzene

: 38962-91-3
3,7-dimethyl-2,1-benzisoxazole

: 62559-41-5
4-ethyl-3-nitrotoluene

: 102878-76-2
3-ethyl-6-nitrotoluene

: 102878-75-1
2-Ethyl-4-methylnitrobenzene

Guidance literature:: With trifluorormethanesulfonic acid; at 110 ℃; Product distribution; Mechanism; other temp., other nitro derivatives of aromatic hydrocarbons;

Reference yield: 83.0%

: 38962-91-3
3,7-dimethyl-2,1-benzisoxazole

: 1333483-14-9
N-methyll-N-(phenylethylnyl)methanesulfonamide

: N-(4,8-dimethyl-3-oxo-4-phenyl-3,4-dihydroquinolin-2-yl)-N-methylmethanesulfonamide

Guidance literature:: With silver hexafluoroantimonate; 2-(di-tert-butylphosphino)-1,1'-biphenylgold(I) chloride; In dichloromethane; at 50 ℃; for 12h; Reagent/catalyst; Sealed tube;
DOI:10.1002/anie.201912334