Chlorimuron ethyl - analytical standard , CAS No.90982-32-4

CAS: 90982-32-4 Cat. No.: C109992 Summenformel: C15H15ClN4O6S Molekulargewicht: 414.82 EG-Nummer: 618-690-2
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QUALITÄT & REINHEIT Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
Benzoic acid, 2-[[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-, ethyl ester|Chlorimuron ethyl ester|ethyl 2-[[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoate|ethyl 2-[(4-chloranyl-6-methoxy-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate|DPX-F 6025|Ethyl 2-(4-chloro-6-methoxy-2-pyrimidinylcarbamoylsulfamoyl)benzoate|2-[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]-oxomethyl]sulfamoyl]benzoic acid ethyl ester|CHLORIMURON-ETHYL [MI]|ethyl 2-{[(4-chloro-6-methoxypyrimidin-2-yl)carbamoyl]sulfamoyl}benzoate|Ethyl 2-(((((4-chloro-6-methoxy-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)benzoate|Ethyl 2-(((((4-chloro-6-methoxyprimidin-2-yl)amino)carbonyl)amino)sulfonyl)benzoate|Chlorimuron ethyl|ethyl 2-({[(4-chloro-6-methoxypyrimidin-2-yl)carbamoyl]amino}sulfonyl)benzoate|ethyl 2-(N-(4-chloro-6-methoxypyrimidin-2-ylcarbamoyl)sulfamoyl)benzoate|Benzoic acid, 2-(((((4-chloro-6-methoxy-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)-, ethyl ester|ethyl 2-[({[(4-chloro-6-methoxypyrimidin-2-yl)amino]carbonyl}amino)sulfonyl]benzoate|2-[[(4-chloro-6-methoxypyrimidin-2-yl)aminocarbonyl]aminosulfonyl]benzoic acid ethyl ester|Chlorimuron-ethyl [ISO]|Ethyl 2-(((4-chloro-6-methoxypyrimidine-2-yl)aminocarbonyl)aminosulfonyl)benzoate|2-(((((4-Chloro-6-methoxy-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)benzoic acid ethyl ester|CHLORIMURON-ETHYL|CHLORIMURON-ETHYL [HSDB]|ethyl 2-[(4-chloro-6-methoxy-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate|ethyl 2-[(4-chloro-6-methoxypyrimidin-2-yl)carbamoylsulfamoyl]benzoate|Classic|2-[[[[(4-CHLORO-6-METHOXY-2-PYRIMIDINYL)AMINO]CARBONYL]AMINO]SULFONYL]BENZOIC ACID ETHYL ESTER
Storage
Room temperature
Shipped In
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Menge
20mg
C109992-20mg
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1 Auf Lager

58,05€

67,60€
Speichern 9,55 € (14.12%)
100mg
C109992-100mg
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3 Auf Lager

229,86€

268,91€
Speichern 39,05 € (14.52%)
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Spezifikationen

Synonyme
Benzoic acid, 2-[[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]-, ethyl ester | Chlorimuron ethyl ester | ethyl 2-[[[[(4-chloro-6-methoxy-2-pyrimidinyl)amino]carbonyl]amino]sulfonyl]benzoate | ethyl 2-[(4-chloranyl-6-methoxy-pyrimidin-2-yl)carbamoylsulfamoyl]benzoate | DPX-F 6025 | Ethyl 2-(4-chloro-6-methoxy-2-pyrimi Show more
Spezifikationen & Reinheit
analytical standard
Storage
Room temperature
Verschickt in
Normal
Note
Analytischer Standard
Namen und Kennungen
Pubchem Sid
Kanonisches Lächeln
CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)Cl)OC
IUPAC Name
ethyl 2-[(4-chloro-6-methoxypyrimidin-2-yl)carbamoylsulfamoyl]benzoate
InChIKey
NSWAMPCUPHPTTC-UHFFFAOYSA-N
INCHI
1S/C15H15ClN4O6S/c1-3-26-13(21)9-6-4-5-7-10(9)27(23,24)20-15(22)19-14-17-11(16)8-12(18-14)25-2/h4-8H,3H2,1-2H3,(H2,17,18,19,20,22)
Isomere SMILES
CCOC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)Cl)OC
RTECS
DG5095000
Molekulargewicht
414.82
Reaxy-Rn
7448363
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7448363&ln=

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
KlasseOrganonitrogen compounds
SubclassSulfonylureas
Intermediate Tree Nodes Not available
Direct ParentPyrimidinyl-2-sulfonylureas
Alternative Parents Benzenesulfonamides  Benzoic acid esters  Benzenesulfonyl compounds  Benzoyl derivatives  Alkyl aryl ethers  Halopyrimidines  Aryl chlorides  Organosulfonic acids and derivatives  Aminosulfonyl compounds  Heteroaromatic compounds  Organic carbonic acids and derivatives  Carboxylic acid esters  Monocarboxylic acids and derivatives  Azacyclic compounds  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  Organochlorides  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidinyl-2-sulfonylurea - Benzenesulfonamide - Benzoate ester - Benzoic acid or derivatives - Benzenesulfonyl group - Benzoyl - Alkyl aryl ether - Halopyrimidine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Pyrimidine - Benzenoid - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Heteroaromatic compound - Carbonic acid derivative - Carboxylic acid ester - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Azacycle - Ether - Carboxylic acid derivative - Organic oxygen compound - Carbonyl group - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organochloride - Organooxygen compound - Organosulfur compound - Aromatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as pyrimidinyl-2-sulfonylureas. These are aromatic heterocyclic compounds containing a pyrimidine ring which is substituted with a sulfonylurea at the ring 2-position.
External Descriptors Sulfonylurea herbicides
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (nicht menschlich)
ALS Acetolactate synthase (354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa crus-galli (3685 Activities)
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Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Oryctolagus cuniculus (11301 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ILV2 Acetolactate synthase catalytic subunit, mitochondrial (10 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trifolium repens (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dactylis glomerata (15 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cyperus iria (145 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot NumberCertificate TypeDatumArtikel
H2402150H2402150Certificate of AnalysisMay 09, 2026 C109992
H2402151H2402151Certificate of AnalysisMay 09, 2026 C109992
H2402152H2402152Certificate of AnalysisMay 09, 2026 C109992
H2402153H2402153Certificate of AnalysisMay 09, 2026 C109992
H2325340H2325340Certificate of AnalysisMay 12, 2025 C109992
L2516230L2516230Certificate of AnalysisApr 11, 2024 C109992
A2104175A2104175Certificate of AnalysisOct 19, 2022 C109992
Chemische und physikalische Eigenschaften
Schmelzpunkt (°C)186°C
Molekulargewicht414.800 g/mol
XLogP32.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count8
Rotatable Bond Count7
Exact Mass414.04 Da
Monoisotopic Mass414.04 Da
Topological Polar Surface Area145.000 Ų
Heavy Atom Count27
Formal Charge0
Complexity628.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Lösungsrechner
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