Cefditoren Pivoxil - ≥98%(HPLC) , Bacterial penicillin-binding protein inhibitor, CAS No.117467-28-4, Bacterial penicillin-binding protein inhibitor

Name: Cefditoren Pivoxil - ≥98%(HPLC) , Bacterial penicillin-binding protein inhibitor, CAS No.117467-28-4, Bacterial penicillin-binding protein inhibitor
SKU: C153441
Availability: InStock

CAS: 117467-28-4 Cat. No.: C153441 Summenformel: C₂₅H₂₈N₆O₇S₃ Molekulargewicht: 620.71 EG-Nummer: 688-157-7

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GRADE & PURITY ≥98%(HPLC)

Synonyms

AMY39447 | CCRIS 7768 | BS-13853 | Cefditoren pivaloyloxymethyl ester | NSC 759098 | [(2,2-dimethylpropanoyl)oxy]methyl (6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-[(Z)-2-(4-methyl-1,3-thiazol-5-yl)ethenyl]-8-oxo-5-thia-1

Storage

Lagerung bei -20°C

Shipped In

Eistruhe + Eispads

Übersicht Specifications Produkteigenschaften Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Lösungsrechner Bewertungen Häufig gestellte Fragen

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Why this grade

≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Lagerung bei -20°C Ships Eistruhe + Eispads Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Cefditoren Pivoxil ist ein Breitspektrum-Antibiotikum gegen gramnegative und grampositive Bakterien.

Specifications

Synonyme

Spezifikationen & Reinheit

≥98%(HPLC)

Storage

Lagerung bei -20°C

Verschickt in

Eistruhe + Eispads

Aktionsart

INHIBITOR

Mechanismus der Wirkung

Bacterial penicillin-binding protein inhibitor

Reinheit

≥98%(HPLC)

Produkteigenschaften

ALogP	4.7

Namen und Kennungen

Pubchem Sid	504764175
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504764175
Kanonisches Lächeln	CC1=C(SC=N1)C=CC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)OCOC(=O)C(C)(C)C
IUPAC Name	2,2-dimethylpropanoyloxymethyl (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(Z)-2-(4-methyl-1,3-thiazol-5-yl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
InChIKey	AFZFFLVORLEPPO-UVYJNCLZSA-N
INCHI	1S/C25H28N6O7S3/c1-12-15(41-10-27-12)7-6-13-8-39-21-17(29-19(32)16(30-36-5)14-9-40-24(26)28-14)20(33)31(21)18(13)22(34)37-11-38-23(35)25(2,3)4/h6-7,9-10,17,21H,8,11H2,1-5H3,(H2,26,28)(H,29,32)/b7-6-,30-16-/t17-,21-/m1/s1
Isomere SMILES	CC1=C(SC=N1)/C=C\C2=C(N3[C@@H]([C@@H](C3=O)NC(=O)/C(=N\OC)/C4=CSC(=N4)N)SC2)C(=O)OCOC(=O)C(C)(C)C
Molekulargewicht	620.71
Reaxy-Rn	37811616
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=37811616&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Klasse Lactams
    - Subclass Beta lactams
      - Ebene5 Cephems
        Ebene6 Cephalosporins

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Klasse	Lactams
Subclass	Beta lactams
Intermediate Tree Nodes	Cephems
Direct Parent	Cephalosporins
Alternative Parents	N-acyl-alpha amino acids and derivatives 2,4-disubstituted thiazoles 4,5-disubstituted thiazoles Acylals 1,3-thiazines 2-amino-1,3-thiazoles Dicarboxylic acids and derivatives Heteroaromatic compounds Enoate esters Tertiary carboxylic acid amides Azetidines Secondary carboxylic acid amides Thiohemiaminal derivatives Dialkylthioethers Azacyclic compounds Acetals Hydrocarbon derivatives Carbonyl compounds Primary amines Organic oxides Organopnictogen compounds
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Cephalosporin - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - 2,4-disubstituted 1,3-thiazole - 4,5-disubstituted 1,3-thiazole - Acylal - Meta-thiazine - Dicarboxylic acid or derivatives - 1,3-thiazol-2-amine - Heteroaromatic compound - Tertiary carboxylic acid amide - Thiazole - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Azole - Carboxylic acid ester - Carboxamide group - Secondary carboxylic acid amide - Amino acid or derivatives - Azetidine - Acetal - Azacycle - Dialkylthioether - Hemithioaminal - Carboxylic acid derivative - Thioether - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Amine - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as cephalosporins. These are compounds containing a 1,2-thiazine fused to a 2-azetidinone to for a oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid moiety or a derivative thereof.
External Descriptors	carboxylic ester
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

Zugehörige Ziele (menschlich)

VDR Tclin Vitamin D receptor (26531 Activities)

Discover Target: VDR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

Discover Target: CYP3A4

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Homo sapiens (32628 Activities)

Lot Number	Certificate Type	Datum	Artikel
I2206471	Certificate of Analysis	Jun 15, 2022	C153441
I2206475	Certificate of Analysis	Jun 15, 2022	C153441
I2206589	Certificate of Analysis	Jun 15, 2022	C153441
I2206590	Certificate of Analysis	Jun 15, 2022	C153441

Löslichkeit	Insoluble in water; Slightly soluble in Methanol; Very slightly soluble in Ethanol; Insoluble in Ether
Spezifische Drehung [α]	-48.5° (C=0.5,MeOH)
Schmelzpunkt (°C)	209 °C(dec.)
Molekulargewicht	620.700 g/mol
XLogP3	4.700
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	14
Rotatable Bond Count	12
Exact Mass	620.118 Da
Monoisotopic Mass	620.118 Da
Topological Polar Surface Area	257.000 Å²
Heavy Atom Count	41
Formal Charge	0
Complexity	1160.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	2
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	2
Covalently-Bonded Unit Count	1

Cefditoren Pivoxil - ≥98%(HPLC) , Bacterial penicillin-binding protein inhibitor, CAS No.117467-28-4, Bacterial penicillin-binding protein inhibitor

Why this grade

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

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