Cefonicid Sodium
Tier C — Watch / tradeCefonicid Sodium
Targets:PBPs
Brand:Monocid
Indications (approved):Bacterial infection
Regional status
Synthetic routes & intermediates5 routes
Routes are ordered originator first, then optimised / process (non-patent) routes; each lists steps, overall yield and the intermediate table (code / CAS / name) — ready for supplier sourcing and RFQ. Rendered by this site from structured data; no third-party route graphics used.
| Code | CAS No. | Intermediate |
|---|---|---|
| Cefonicid-016 | 957-68-6 | (6R,7R)-3-(Acetoxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-017 | - | Bis(sodium)bis[(5-sulfanyl-1H-tetrazol-1-yl)methanesulfonate] |
| Cefonicid-012 | 61270-71-1 | (6R,7R)-7-Amino-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-015 | 29169-64-0 | Formic acid 2-chloro-2-oxo-1(R)-phenylethyl ester<-fgf->O-Formyl-D-mandelic acid chloride<-fgf->D-O-Formylmandeolyl chloride |
| Cefonicid-018 | 159276-97-8 | (6R,7R)-7-[[(2R)-2-Hydroxy-2-phenylacetyl]amino]-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid - N,N'-dibenzylethane-1,2-diamine |
| Code | CAS No. | Intermediate |
|---|---|---|
| Cefonicid-001 | 13881-91-9 | aminomethanesulfonic acid |
| Cefonicid-002 | 85-44-9Available | Phthalic anhydride |
| Cefonicid-003 | 250654-34-3 | (1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)methanesulfonic acid |
| Cefonicid-004 | 61271-03-2 | (1,3-dioxoisoindol-2-yl)methanesulfonyl chloride |
| Cefonicid-005 | - | (5-sulfanyl-1H-1,2,3,4-tetrazol-1-yl)methanesulfonic acid |
| Cefonicid-006 | - | N-tert-butyl-1-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)methanesulfonamide |
| Cefonicid-007 | - | 1-amino-N-tert-butylmethanesulfonamide |
| Cefonicid-008 | - | N-tert-butyl-1-{[(methylsulfanyl)methanethioyl]amino}methanesulfonamide |
| Cefonicid-009 | - | N-tert-butyl-1-(5-sulfanyl-1H-1,2,3,4-tetrazol-1-yl)methanesulfonamide |
| Cefonicid-010 | 751425-57-7 | {[(methylsulfanyl)methanethioyl]amino}methanesulfonic acid |
| Cefonicid-011 | 957-68-6 | (6R,7R)-3-(Acetoxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-012 | 61270-71-1 | (6R,7R)-7-Amino-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-013 | 40512-60-5 | (1R)-2-Chloro-2-oxo-1-phenylethyl dichloroacetate |
| Cefonicid-014 | 51818-85-0 | (6R,7R)-3-[(Acetyloxy)methyl]-7-[[(2R)-2-hydroxy-2-phenylacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-015 | 29169-64-0 | Formic acid 2-chloro-2-oxo-1(R)-phenylethyl ester<-fgf->O-Formyl-D-mandelic acid chloride<-fgf->D-O-Formylmandeolyl chloride |
| Code | CAS No. | Intermediate |
|---|---|---|
| Cefonicid-019 | 145125-45-7 | (6R,7R)-7-[[(2R)-2-(Formyloxy)-2-phenylacetyl]amino]-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-020 | 61270-58-4 | (6R,7R)-7-[[(2R)-2-Hydroxy-2-phenylacetyl]amino]-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-012 | 61270-71-1 | (6R,7R)-7-Amino-8-oxo-3-([[1-(sulfomethyl)-1H-tetrazol-5-yl]sulfanyl]methyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid |
| Cefonicid-015 | 29169-64-0 | Formic acid 2-chloro-2-oxo-1(R)-phenylethyl ester<-fgf->O-Formyl-D-mandelic acid chloride<-fgf->D-O-Formylmandeolyl chloride |
| Code | CAS No. | Intermediate |
|---|---|---|
| Cefonicid-021 | 613-90-1 | Oxo(phenyl)acetonitrile |
| Cefonicid-022 | 611-73-4 | 2-Oxo-2-phenylacetic acid |
| Cefonicid-023 | 611-71-2 | (2R)-Hydroxy(phenyl)acetic acid |
| Cefonicid-024 | 29169-63-9 | (2R)-(Formyloxy)(phenyl)acetic acid |
| Cefonicid-015 | 29169-64-0 | Formic acid 2-chloro-2-oxo-1(R)-phenylethyl ester<-fgf->O-Formyl-D-mandelic acid chloride<-fgf->D-O-Formylmandeolyl chloride |
| Code | CAS No. | Intermediate |
|---|---|---|
| Cefonicid-025 | - | Hydroxy(phenyl)acetonitrile |
| Cefonicid-023 | 611-71-2 | D-Mandelic acid |
Frequently asked questions
What are the approved indications of Cefonicid Sodium?
Approved indications include: Bacterial infection.
When does the Cefonicid Sodium patent expire?
No public expiry year is available for Cefonicid Sodium yet; this page updates once verified.
How many synthesis routes are recorded for Cefonicid Sodium?
5 synthesis routes are recorded; the shortest is 1 steps with / total yield. Intermediates in each route carry codes and CAS numbers.
Where can I buy Cefonicid Sodium intermediates?
1 intermediate CAS of Cefonicid Sodium are available through the Unibest supply network — see the route tables on this page and request a quote per CAS.
How do I get a quote for Cefonicid Sodium intermediates?
Open the CAS profile of the target intermediate from this page, or submit an RFQ directly — the CAS enters the matching flow automatically and the supply network responds with quotes.
Source: cross-verified data (structured fields only) · 2026-09-29