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CAS

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874752-05-3

(2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL is a chemical compound with a molecular formula C15H11NO3. It is a derivative of 5-nitroindole, which is a type of heterocyclic compound. (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL consists of a phenyl group attached to a methanol group, with a 5-nitro-1H-indol-2-yl group attached to the phenyl ring. Due to its unique structure and potential pharmacological properties, it may be used in organic synthesis or as a research compound. However, it is important to handle this compound with care, as it may have toxic or potentially harmful properties.

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  • 874752-05-3 Structure

  • Basic information

    1. Product Name: (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL
    2. Synonyms: (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL
    3. CAS NO:874752-05-3
    4. Molecular Formula: C15H12N2O3
    5. Molecular Weight: 268.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874752-05-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL(874752-05-3)
    11. EPA Substance Registry System: (2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL(874752-05-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 874752-05-3(Hazardous Substances Data)

874752-05-3 Usage

Uses

Used in Organic Synthesis:
(2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows it to be a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research Compounds:
(2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL is used as a research compound in the field of chemistry and pharmaceuticals. Its unique structure and potential pharmacological properties make it a promising candidate for studying various chemical reactions and exploring its potential applications in drug discovery and development.
Used in Pharmaceutical Industry:
(2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structure and potential pharmacological properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
(2-(5-NITRO-1H-INDOL-2-YL)PHENYL)METHANOL is used as a chemical intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure allows it to be a key component in the development of new and effective agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 874752-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,7,5 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 874752-05:
(8*8)+(7*7)+(6*4)+(5*7)+(4*5)+(3*2)+(2*0)+(1*5)=203
203 % 10 = 3
So 874752-05-3 is a valid CAS Registry Number.

874752-05-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(5-nitro-1H-indol-2-yl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,2-(5-nitro-1H-indol-2-yl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:874752-05-3 SDS

874752-05-3Relevant articles and documents

Structure-activity relationships of 2-aryl-1H-indole inhibitors of the NorA efflux pump in Staphylococcus aureus

Ambrus, Joseph I.,Kelso, Michael J.,Bremner, John B.,Ball, Anthony R.,Casadei, Gabriele,Lewis, Kim

scheme or table, p. 4294 - 4297 (2009/04/06)

The synthesis of 22 2-aryl-1H-indoles, including 12 new compounds, has been achieved via Pd- or Rh-mediated methodologies, or selective electrophilic substitution. All three methods were based on elaborations from simple indole precursors. SAR studies on

Synthesis of functionalised 2-aryl-5-nitro-1H-indoles and their activity as bacterial NorA efflux pump inhibitors

Samosorn, Siritron,Bremner, John B.,Ball, Anthony,Lewis, Kim

, p. 857 - 865 (2007/10/03)

In order to develop structure-activity relationships and to provide access to antibacterial agents for dual action studies, a variety of aryl group-substituted 2-aryl-5-nitro-1H-indoles were synthesized and the activity of the compounds assessed as inhibitors of the NorA multidrug resistance pump in the bacterium Staphylococcus aureus. The NorA protein from the major facilitator superfamily of efflux pumps confers resistance to a variety of structurally dissimilar antimicrobials such as norfloxacin, ethidium bromide, berberine and acriflavin. The compound [4-benzyloxy-2-(5-nitro-1H-2-yl)-phenyl]-methanol was the most potent pump inhibitor.

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