Isobutyl methacrylate - ≥99%, contains MEHQ as stabilizer , CAS No.97-86-9

CAS: 97-86-9 Cat. No.: I106679 Formula: C₈H₁₄O₂ Peso molecolare: 142.2 Beilstein Registry Number: 1747595 Numero EC: 202-613-0

QUALITÀ & PUREZZA ≥99%, contains MEHQ as stabilizer

Synonyms

ISOBUTYL METHACRYLATE [INCI] | DTXSID3025461 | EINECS 202-613-0 | NCGC00259117-01 | Isobutyl 2-methylacrylate # | 2-methylpropyl 2-methylprop-2-enoate | MFCD00084435 | AKOS005622614 | Isobutylmethacrylate | NCGC00091087-01 | M0132 | MFCD00008931 | CAS-97-

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Specifiche

Sinonimi

ISOBUTYL METHACRYLATE [INCI] | DTXSID3025461 | EINECS 202-613-0 | NCGC00259117-01 | Isobutyl 2-methylacrylate # | 2-methylpropyl 2-methylprop-2-enoate | MFCD00084435 | AKOS005622614 | Isobutylmethacrylate | NCGC00091087-01 | M0132 | MFCD00008931 | CAS-97-

Specifiche e purezza

≥99%, contains MEHQ as stabilizer

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice,FedEx DG Service

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

508814858

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508814858

Sorrisi canonici

CC(C)COC(=O)C(=C)C

IUPAC Name

2-methylpropyl 2-methylprop-2-enoate

InChIKey

RUMACXVDVNRZJZ-UHFFFAOYSA-N

INCHI

1S/C8H14O2/c1-6(2)5-10-8(9)7(3)4/h6H,3,5H2,1-2,4H3

Isomeri SMILES

CC(C)COC(=O)C(=C)C

WGK Germania

1

RTECS

OZ4900000

Numero UN

2283

Gruppo di imballaggio

III

Peso molecolare

142.2

Beilstein

1747595

Reaxy-Rn

1747595

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1747595&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid esters
          • Level6 Alpha,beta-unsaturated carboxylic esters
            • Level7 Enoate esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid esters - Alpha,beta-unsaturated carboxylic esters
• Direct Parent: Enoate esters
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Enoate ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as enoate esters. These are an alpha,beta-unsaturated carboxylic ester of general formula R1C(R2)=C(R3)C(=O)OR4 (R4= organyl compound) in which the ester C=O function is conjugated to a C=C double bond at the alpha,beta position.
• 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

Obiettivi associati (umani)

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

TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)

Discover Target: TSHR

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

Obiettivi associati (non umani)

Plasmodium falciparum (966862 Activities)

Explore this target

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

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solubility in water: Practically insoluble; Miscible with Ether,Ethanol
• Indice di rifrazione: 1.4199
• Punto di infiammabilità (°F): 107.6 °F
• Punto di infiammabilità (°C): 49℃
• Punto di ebollizione (°C): 155°C
• Punto di fusione (°C): -37°C
• Peso molecolare: 142.200 g/mol
• XLogP3: 2.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 142.099 Da
• Monoisotopic Mass: 142.099 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 136.000
• 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