Indoxyl acetate - ≥97% , CAS No.608-08-2

CAS: 608-08-2 Cat. No.: I107160 Formula: C₁₀H₉NO₂ Peso molecolare: 175.18 Beilstein Registry Number: 143086 Numero EC: 210-154-2

GRADE & PURITY ≥97%

Synonyms

HY-137884 | I-5600 | NSC13964 | NSC-13964 | SY059874 | CHEBI:169991 | FT-0615876 | Indoxyl acetate | Indol-3-ol, acetate | 1H-Indol-3-yl acetate | 3-Indolyl acetate | MFCD00014561 | DTXSID6060559 | 1H-Indol-3-ol, 3-acetate | EINECS 210-154-2 | Indoxyl ace

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

Indoxyl acetate has been used as a colorimetric substrate for differentiating esterases from various microbiological species.

Application：

ndoxyl acetate:

has been used to prepare free indoxyl for fermentor feeds and for in vitro 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) synthase inactivation assays；

may be used as the potential substrate for the evaluation of carbonic anhydrases (CAs) esterase activity；

may be used to prepare indoxyl acetate differential disk to evaluate the indoxyl acetate hydrolysis test for the differentiation of Campylobacter species；

Specifications

Sinonimi

HY-137884 | I-5600 | NSC13964 | NSC-13964 | SY059874 | CHEBI:169991 | FT-0615876 | Indoxyl acetate | Indol-3-ol, acetate | 1H-Indol-3-yl acetate | 3-Indolyl acetate | MFCD00014561 | DTXSID6060559 | 1H-Indol-3-ol, 3-acetate | EINECS 210-154-2 | Indoxyl ace

Specifiche e purezza

≥97%

Meccanismi biochimici e fisiologici

Indoxyl acetate (IA) can be used as a substrate to detect acetylcholinesterase (AChE) activity. It may also have the potential to be used as a suitable substrate for fast and easy detection of lipase activity；

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

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

Purezza

≥97%

Nomi e identificatori

Pubchem Sid

508812938

Sorrisi canonici

CC(=O)OC1=CNC2=CC=CC=C21

IUPAC Name

1H-indol-3-yl acetate

InChIKey

JBOPQACSHPPKEP-UHFFFAOYSA-N

INCHI

1S/C10H9NO2/c1-7(12)13-10-6-11-9-5-3-2-4-8(9)10/h2-6,11H,1H3

Isomeri SMILES

CC(=O)OC1=CNC2=CC=CC=C21

WGK Germania

3

RTECS

AI3325000

Peso molecolare

175.18

Beilstein

143086

Reaxy-Rn

143086

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=143086&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Indoles and derivatives
      • Subclass Indoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Indoles and derivatives
• Subclass: Indoles
• Intermediate Tree Nodes: Not available
• Direct Parent: Indoles
• Alternative Parents: Substituted pyrroles Benzenoids Heteroaromatic compounds Carboxylic acid esters Monocarboxylic acids and derivatives Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indole - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Carboxylic acid ester - Azacycle - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
• 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 (non umani)

Slc22a6 Solute carrier family 22 member 6 (141 Activities)

Discover Target: Slc22a6

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in ethanol, water, chloroform, dichloromethane and methanol.
• Sensibilità: Moisture & air & light sensitive
• Punto di fusione (°C): 128-131°C
• Peso molecolare: 175.180 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 175.063 Da
• Monoisotopic Mass: 175.063 Da
• Topological Polar Surface Area: 42.100 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 205.000
• 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