(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Base Information

Chemical Name:(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester
CAS No.:91775-99-4
Molecular Formula:C₃₂H₂₇N₇O₅S₄
Molecular Weight:717.874
Hs Code.:

(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Synonyms:(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Suppliers and Price of (R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

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
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

There total 6 articles about (R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester 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: 78.0%

: 120-78-5
di(benzothiazol-2-yl)disulfide

: 91530-67-5
(R)-2-((1R,5R)-3-Benzoyl-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

: 91775-99-4
(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Guidance literature:: With perchloric acid; In tetrahydrofuran; for 50h; Ambient temperature;
DOI:10.1016/S0040-4039(01)90045-0

Reference yield:

: 91530-64-2
(R)-2-((1R,5R)-3-Benzoyl-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-3-methyl-but-3-enoic acid benzyl ester

: 91775-99-4
(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / NaCl, H₂SO₄ / CHCl₃; 2-methyl-propan-2-ol; H₂O / electrolytic chlorination

2: NaI / acetone / Heating

3: acetone

4: 78 percent / aqueous 10percent HClO₄ / tetrahydrofuran / 50 h / Ambient temperature

With perchloric acid; sulfuric acid; sodium iodide; sodium chloride; In tetrahydrofuran; chloroform; water; acetone; tert-butyl alcohol;
DOI:10.1016/S0040-4039(01)90045-0

Reference yield:

: 91530-65-3
(R)-2-((1R,5R)-3-Benzoyl-7-oxo-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-3-chloromethyl-but-3-enoic acid benzyl ester

: 91775-99-4
(R)-2-[(2R,3R)-2-(Benzothiazol-2-yldisulfanyl)-4-oxo-3-(2-oxo-2-phenyl-acetylamino)-azetidin-1-yl]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-but-3-enoic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: NaI / acetone / Heating

2: acetone

3: 78 percent / aqueous 10percent HClO₄ / tetrahydrofuran / 50 h / Ambient temperature

With perchloric acid; sodium iodide; In tetrahydrofuran; acetone;
DOI:10.1016/S0040-4039(01)90045-0