cloxacillin sodium

Base Information

Chemical Name:cloxacillin sodium
CAS No.:7060-81-3
Molecular Formula:C₁₉H₁₈ClN₃O₅S
Molecular Weight:435.888
Hs Code.:
Mol file:7060-81-3.mol

Synonyms:4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-

Suppliers and Price of cloxacillin sodium

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 3 raw suppliers

Chemical Property of cloxacillin sodium

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of cloxacillin sodium

There total 7 articles about cloxacillin sodium 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:

: 3717-28-0
2-chloro benzaldehyde oxime

: 61-72-3,7060-81-3
cloxacillin

Guidance literature:: Multi-step reaction with 5 steps

1: Cl₂

2: (i) Na, MeOH, (ii) /BRN= 2502600/

3: aq. KOH / ethanol

4: SOCl₂

5: aq. NaOH, isobutyl methyl ketone

With potassium hydroxide; sodium hydroxide; thionyl chloride; chlorine; 4-methyl-2-pentanone; In ethanol;
DOI:10.1039/jr9630005838

Reference yield:

: 4357-94-2
methyl 3-(2'-chlorophenyl)-5-methylisoxazole-4-carboxylate

: 61-72-3,7060-81-3
cloxacillin

Guidance literature:: Multi-step reaction with 3 steps

1: aq. KOH / ethanol

2: SOCl₂

3: aq. NaOH, isobutyl methyl ketone

With potassium hydroxide; sodium hydroxide; thionyl chloride; 4-methyl-2-pentanone; In ethanol;
DOI:10.1039/jr9630005838

Reference yield:

: 29568-74-9
2-chloro-N-hydroxybenzimidoyl chloride

: 61-72-3,7060-81-3
cloxacillin

Guidance literature:: Multi-step reaction with 4 steps

1: (i) Na, MeOH, (ii) /BRN= 2502600/

2: aq. KOH / ethanol

3: SOCl₂

4: aq. NaOH, isobutyl methyl ketone

With potassium hydroxide; sodium hydroxide; thionyl chloride; 4-methyl-2-pentanone; In ethanol;
DOI:10.1039/jr9630005838