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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Fenobucarb solution - analytical standard, 1.00mg/ml in methanol , CAS No.3766-81-2
GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods. 1.00mg/ml in methanol Synonyms
2-sec-Butylphenyl N-methylcarbamate | Methyl-carbamic acid 2-sec-butyl-phenyl ester | SY110156 | (2-butan-2-ylphenyl) N-methylcarbamate | 5MS2P7M0CF | Fenobucarb | SCHEMBL73674 | Hopcin | Bayer 41637 | FENOBUCARB [ISO] | DIRFUJHNVNOBMY-UHFFFAOYSA- | Fenob
Storage
Store at 2-8°C,Protected from light
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Why this grade analytical standard, 1.00mg/ml in methanol Étalon d'analyse for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light Ships Wet ice 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 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
2-sec-Butylphenyl N-methylcarbamate | Methyl-carbamic acid 2-sec-butyl-phenyl ester | SY110156 | (2-butan-2-ylphenyl) N-methylcarbamate | 5MS2P7M0CF | Fenobucarb | SCHEMBL73674 | Hopcin | Bayer 41637 | FENOBUCARB [ISO] | DIRFUJHNVNOBMY-UHFFFAOYSA- | Fenob
Spécifications et pureté
analytical standard, 1.00mg/ml in methanol
Conditions de stockage de stockage
Store at 2-8°C,Protected from light
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Sourires canoniques
CCC(C)C1=CC=CC=C1OC(=O)NC
IUPAC Name
(2-butan-2-ylphenyl) N-methylcarbamate
InChIKey
DIRFUJHNVNOBMY-UHFFFAOYSA-N
INCHI
1S/C12H17NO2/c1-4-9(2)10-7-5-6-8-11(10)15-12(14)13-3/h5-9H,4H2,1-3H3,(H,13,14)
Isomères SMILES
CCC(C)C1=CC=CC=C1OC(=O)NC
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2052332&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.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Classe Benzene and substituted derivatives Subclass Phenyl methylcarbamates Intermediate Tree Nodes Not available Direct Parent Phenyl methylcarbamates Alternative Parents Phenylpropanes Phenoxy compounds Carbamate esters Organic carbonic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Phenyl methylcarbamate - Phenylpropane - Phenoxy compound - Carbamic acid ester - Carbonic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as phenyl methylcarbamates. These are aromatic compounds containing a methylcarbamic acid esterified with a phenyl group. External Descriptors Carbamate insecticides Data sources 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Sensibilité Light sensitive. Poids moléculaire 207.270 g/mol XLogP3 2.800 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 4 Exact Mass 207.126 Da Monoisotopic Mass 207.126 Da Topological Polar Surface Area 38.300 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 206.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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