Poly(hydroxypropyl methacrylate) - crystalline , CAS No.9086-85-5

CAS: 9086-85-5 Cat. No.: P477445 Fórmula: (C₇H₁₂O₃)n

GRADE & PURITY crystalline

Synonyms

2-hydroxy-3-propyl methacrylate | Acryester HP | NCGC00260080-01 | Hydroxypropyl methacrylate, mixture of isomers | W-100292 | 2-hydroxy-n-propyl methacrylate | DSSTox_GSID_25934 | DSSTox_RID_78619 | DSSTox_GSID_27936 | NCGC00258784-01 | .beta.-hydroxypro

Storage

Room temperature

Visão geral

Description

Preparation instructions

Form

Water-swellable polymer. Hydrogel.

Principle

Specifications

Sinónimos

2-hydroxy-3-propyl methacrylate | Acryester HP | NCGC00260080-01 | Hydroxypropyl methacrylate, mixture of isomers | W-100292 | 2-hydroxy-n-propyl methacrylate | DSSTox_GSID_25934 | DSSTox_RID_78619 | DSSTox_GSID_27936 | NCGC00258784-01 | .beta.-hydroxypro

Especificações e pureza

crystalline

Condições de armazenamento de armazenamento

Room temperature

Nomes e identificadores

Sorrisos canónicos

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

IUPAC Name

2-hydroxypropyl 2-methylprop-2-enoate

InChIKey

VHSHLMUCYSAUQU-UHFFFAOYSA-N

INCHI

1S/C7H12O3/c1-5(2)7(9)10-4-6(3)8/h6,8H,1,4H2,2-3H3

SMILES isoméricas

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

Reaxy-Rn

1752228

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1752228&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: Secondary alcohols Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Enoate ester - Secondary alcohol - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrição: 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: enoate ester

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

Alvos associados (humanos)

AR Tclin Androgen Receptor (11781 Activities)

Discover Target: AR

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

Mecanismos de ação

Propriedades químicas e físicas

• Ponto de inflamação (°F): Not applicable
• Ponto de inflamação (°C): Not applicable
• Peso molecular: 144.170 g/mol
• XLogP3: 1.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 144.079 Da
• Monoisotopic Mass: 144.079 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 140.000
• 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