N-BOC 4-bromo-2-metilanilina - ≥98% , CAS No.306937-14-4

CAS: 306937-14-4 Cat. No.: N183572 Peso molecular: 286.2

GRADE & PURITY ≥98%

Synonyms

Carbamic acid, (4-bromo-2-methylphenyl)-, 1,1-dimethylethyl ester (9CI) | EN300-202984 | Carbamic acid, N-(4-bromo-2-methylphenyl)-, 1,1-dimethylethyl ester | tert-Butyl (4-bromo-2-methylphenyl)carbamate | ZMUXMKPOXRAYSP-UHFFFAOYSA-N | tert-Butyl 4-bromo-

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

Carbamic acid, (4-bromo-2-methylphenyl)-, 1, 1-dimethylethyl ester (9CI) | EN300-202984 | Carbamic acid, N-(4-bromo-2-methylphenyl)-, 1, 1-dimethylethyl ester | tert-Butyl (4-bromo-2-methylphenyl)carbamate | ZMUXMKPOXRAYSP-UHFFFAOYSA-N | tert-Butyl 4-bromo-

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Sonrisas canónicas: CC1=C(C=CC(=C1)Br)NC(=O)OC(C)(C)C
• IUPAC Name: tert-butyl N-(4-bromo-2-methylphenyl)carbamate
• InChIKey: ZMUXMKPOXRAYSP-UHFFFAOYSA-N
• INCHI: 1S/C12H16BrNO2/c1-8-7-9(13)5-6-10(8)14-11(15)16-12(2,3)4/h5-7H,1-4H3,(H,14,15)
• Isómeros SMILES: CC1=C(C=CC(=C1)Br)NC(=O)OC(C)(C)C
• Peso molecular: 286.2
• Reaxy-Rn: 10252992
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=10252992&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenylcarbamic acid esters

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenylcarbamic acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylcarbamic acid esters
• Alternative Parents: Toluenes Bromobenzenes Aryl bromides Carbamate esters Organic carbonic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenylcarbamic acid ester - Bromobenzene - Halobenzene - Toluene - Aryl bromide - Aryl halide - Carbamic acid ester - Carbonic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenylcarbamic acid esters. These are ester derivatives of phenylcarbamic acids.
• External Descriptors: Not available

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.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Peso molecular: 286.160 g/mol
• XLogP3: 3.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 285.036 Da
• Monoisotopic Mass: 285.036 Da
• Topological Polar Surface Area: 38.300 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 250.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1