1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate

Base Information

Chemical Name:1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate
CAS No.:215789-59-6
Molecular Formula:C₁₅H₁₁F₃N₂O₃S
Molecular Weight:356.325
Hs Code.:
DSSTox Substance ID:DTXSID801172903

Synonyms:DTXSID801172903;1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate;215789-59-6

Suppliers and Price of 1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate

Supply Marketing:

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

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Chemical Property of 1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:356.04424788
Heavy Atom Count:24
Complexity:529

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C3=CC=CC=C3C(=N2)OS(=O)(=O)C(F)(F)F

Technology Process of 1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate

There total 3 articles about 1-(Phenylmethyl)-1H-indazol-3-yl 1,1,1-trifluoromethanesulfonate 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: 95.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 2215-63-6
1-benzyl-1,2-dihydro-3H-indazol-3-one

: 215789-59-6
Trifluoro-methanesulfonic acid 1-benzyl-1H-indazol-3-yl ester

Guidance literature:: With pyridine; In dichloromethane;
DOI:10.1055/s-1998-1882

Reference yield:

: 7364-25-2
3-indazolinone

: 215789-59-6
Trifluoro-methanesulfonic acid 1-benzyl-1H-indazol-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / NaOH / ethanol

2: 95 percent / pyridine / CH₂Cl₂

With pyridine; sodium hydroxide; In ethanol; dichloromethane;
DOI:10.1055/s-1998-1882

Reference yield:

: 100-44-7
benzyl chloride

: 215789-59-6
Trifluoro-methanesulfonic acid 1-benzyl-1H-indazol-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / NaOH / ethanol

2: 95 percent / pyridine / CH₂Cl₂

With pyridine; sodium hydroxide; In ethanol; dichloromethane;
DOI:10.1055/s-1998-1882