Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate

Base Information

Chemical Name:Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate
CAS No.:62029-64-5
Molecular Formula:C₁₃H₁₀ClNOSe
Molecular Weight:310.642
Hs Code.:
DSSTox Substance ID:DTXSID401214648

Synonyms:62029-64-5;Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate;DTXSID401214648

Suppliers and Price of Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate

Supply Marketing:

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

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Chemical Property of Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:310.96161
Heavy Atom Count:17
Complexity:266

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)[Se]C(=O)C2=C(N=CC=C2)Cl

Technology Process of Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate

There total 5 articles about Se-(4-Methylphenyl) 2-chloro-3-pyridinecarboselenoate 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:

: 2942-59-8
2-chloronicotinic acid

: 62029-64-5
4-methylphenyl ester of 2-chloro-selenonicotin acid

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / benzene / 1 h / Heating

2: benzene; ethanol; H₂O

With thionyl chloride; In ethanol; water; benzene;
DOI:10.1016/S0022-328X(00)83485-3

Reference yield:

: 21856-94-0
di-p-tolyl diselenide

: 62029-64-5
4-methylphenyl ester of 2-chloro-selenonicotin acid

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄, aq. NaOH / benzene; ethanol / Heating

2: benzene; ethanol; H₂O

With sodium hydroxide; sodium tetrahydroborate; In ethanol; water; benzene;
DOI:10.1016/S0022-328X(00)83485-3

Reference yield:

: 73831-79-5
2-(4-methylphenylseleno)-selenonicotinacid-Se-4-methylphenylester

: 62029-64-5
4-methylphenyl ester of 2-chloro-selenonicotin acid

Guidance literature:: Multi-step reaction with 3 steps

1: 440 mg / benzene / Irradiation

2: NaBH₄, aq. NaOH / benzene; ethanol / Heating

3: benzene; ethanol; H₂O

With sodium hydroxide; sodium tetrahydroborate; In ethanol; water; benzene;
DOI:10.1016/S0022-328X(00)83485-3