1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide

Base Information

Chemical Name:1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide
CAS No.:51176-79-5
Molecular Formula:C14H11NO3S
Molecular Weight:273.312
Hs Code.:
DSSTox Substance ID:DTXSID30351375
Nikkaji Number:J881.253E
Wikidata:Q82127753
ChEMBL ID:CHEMBL1702896
Mol file:51176-79-5.mol

Synonyms:51176-79-5;1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide;CDS1_004053;CBMicro_017557;3-(benzyloxy)-1,2-benzothiazole 1,1-dioxide;Oprea1_196936;DivK1c_005093;CHEMBL1702896;DTXSID30351375;CCG-6197;STK731689;AKOS003224900;NCGC00188409-01;BIM-0017469.P001;EU-0071208;SR-01000430929;SR-01000430929-1;3-(BENZYLOXY)-1H-1,2-BENZISOTHIAZOLE-1,1-DIONE

Suppliers and Price of 1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide

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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Total 0 raw suppliers

Chemical Property of 1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide

Chemical Property:

PSA：64.11000
LogP:2.86870
XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:273.04596439
Heavy Atom Count:19
Complexity:446

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=NS(=O)(=O)C3=CC=CC=C32

Technology Process of 1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide

There total 6 articles about 1,2-Benzisothiazole, 3-(phenylmethoxy)-, 1,1-dioxide 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: 72.0%

: 567-19-1
3-chloro-1,2-benzisothiazole 1,1-dioxide

: 100-51-6,185532-71-2
benzyl alcohol

: 51176-79-5
3-Benzyloxy-1,2-benzisothiazole 1,1-dioxide

Guidance literature:: With triethylamine; In toluene; for 0.75h; Heating;

Reference yield: 59.0%

: 128-44-9
saccharin sodium salt

: 100-51-6,185532-71-2
benzyl alcohol

: 51176-79-5
3-Benzyloxy-1,2-benzisothiazole 1,1-dioxide

: 3416-59-9
N-benzylsaccharin

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 16h;
DOI:10.1002/ejoc.200600508

Reference yield: 41.0%

: 81-07-2
saccharin

: 100-51-6,185532-71-2
benzyl alcohol

: 51176-79-5
3-Benzyloxy-1,2-benzisothiazole 1,1-dioxide

: 3416-59-9
N-benzylsaccharin

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; regioselective reaction;
DOI:10.3184/174751913X13716447161975