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CAS

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20716-26-1

3-(2-NITRO-PHENYL)-PROPAN-1-OL, a chemical compound with the molecular formula C9H11NO3, is a colorless to pale yellow liquid. It has a molecular weight of 189.19 g/mol and is known for its antimicrobial properties. 3-(2-NITRO-PHENYL)-PROPAN-1-OL is commonly used in organic synthesis and as a reagent in chemical reactions, with potential applications in pharmaceuticals and biotechnology. However, it is considered a hazardous chemical and requires careful handling with proper safety precautions.

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  • 20716-26-1 Structure

  • Basic information

    1. Product Name: 3-(2-NITRO-PHENYL)-PROPAN-1-OL
    2. Synonyms: 3-(2-NITRO-PHENYL)-PROPAN-1-OL;2-Nitro-benzenepropanol
    3. CAS NO:20716-26-1
    4. Molecular Formula: C9H11NO3
    5. Molecular Weight: 181.18854
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20716-26-1.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(2-NITRO-PHENYL)-PROPAN-1-OL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(2-NITRO-PHENYL)-PROPAN-1-OL(20716-26-1)
    11. EPA Substance Registry System: 3-(2-NITRO-PHENYL)-PROPAN-1-OL(20716-26-1)

  • 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: 20716-26-1(Hazardous Substances Data)

20716-26-1 Usage

Uses

Used in Organic Synthesis:
3-(2-NITRO-PHENYL)-PROPAN-1-OL is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of new compounds.
Used in Pharmaceutical Industry:
3-(2-NITRO-PHENYL)-PROPAN-1-OL is used as an intermediate in the development of pharmaceuticals due to its potential applications in drug discovery and synthesis.
Used in Biotechnology:
In the biotechnology industry, 3-(2-NITRO-PHENYL)-PROPAN-1-OL is utilized for its antimicrobial properties, which can be harnessed for various applications such as the development of antimicrobial agents.
Used in Chemical Reactions:
3-(2-NITRO-PHENYL)-PROPAN-1-OL is used as a reagent in chemical reactions for its capacity to facilitate specific transformations and processes in the synthesis of target compounds.
Safety Precautions:
Given its classification as a hazardous chemical, 3-(2-NITRO-PHENYL)-PROPAN-1-OL requires careful handling. It is essential to follow proper safety protocols, including the use of personal protective equipment and adherence to guidelines for the storage and disposal of hazardous materials.

Check Digit Verification of cas no

The CAS Registry Mumber 20716-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,1 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20716-26:
(7*2)+(6*0)+(5*7)+(4*1)+(3*6)+(2*2)+(1*6)=81
81 % 10 = 1
So 20716-26-1 is a valid CAS Registry Number.

20716-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-nitrophenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names Benzenepropanol,2-nitro

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:20716-26-1 SDS

20716-26-1Relevant articles and documents

4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES

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Page/Page column 93-94, (2020/11/03)

Compounds of formula (I) for use in the treatment or prophylaxis of a disease, which is a hyperproliferative disease and/or a disorder responsive to induction of cell death, selected from a haematological tumour, a solid tumour and/or metastases thereof, said tumour harbouring a mutant EGFR with exon 19 or 21 mutations, and their use as pharmaceuticals.

4H-PYRROLO[3,2-C]PYRIDIN-4-ONE DERIVATIVES

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Page/Page column 84, (2019/05/15)

Compounds of formula (I) processes for their production and their use as pharmaceuticals.

Proline catalyzed sequential α-aminooxylation or -amination/reductive cyclization of o-nitrohydrocinnamaldehydes: A high yield synthesis of chiral 3-substituted tetrahydroquinolines

Rawat, Varun,Kumar, B. Senthil,Sudalai, Arumugam

supporting information, p. 3608 - 3611 (2013/06/26)

A new sequential organocatalytic method for the synthesis of chiral 3-substituted (X = OH, NH2) tetrahydroquinoline derivatives (THQs) [ee up to 99%, yield up to 87%] based on α-aminooxylation or -amination followed by reductive cyclization of o-nitrohydrocinnamaldehydes has been described. This methodology has been efficiently demonstrated in the synthesis of two important bioactive molecules namely (-)-sumanirole (96% ee) and 1-[(S)-3-(dimethylamino)-3,4-dihydro-6,7-dimethoxy-quinolin-1(2H)-yl]propanone (92% ee). The Royal Society of Chemistry 2013.

Cobalt(II) chloride hexahydrate-diisopropylamine catalyzed mild and chemoselective reduction of carboxylic esters with sodium borohydride

Jagdale, Arun R.,Paraskar, Abhimanyu S.,Sudalai, Arumugam

experimental part, p. 660 - 664 (2009/07/03)

The cobalt-catalyzed reduction of unsaturated α-cyano carboxylic esters using sodium borohydride (NaBH4) leads to the corresponding saturated cyano alcohols in high yields. In particular, the new catalytic system cobalt(II) chloride-diisopropylamine in combination with NaBH4 showed excellent activity in the chemoselective reduction of a variety of carboxylic esters to their corresponding alcohols in good to excellent yields under mild conditions. Georg Thieme Verlag Stuttgart.

Wilkinson's catalyst catalyzed selective hydrogenation of olefin in the presence of an aromatic nitro function: A remarkable solvent effect

Jourdant, Angelique,Gonzalez-Zamora, Eduardo,Zhu, Jieping

, p. 3163 - 3164 (2007/10/03)

Optimal conditions for chlorotris(triphenylphosphine)rhodium(I) (Wilkinson's catalyst) catalyzed selective saturation of a double bond in the presence of a nitro function are developed. Aryl iodide and benzyl ether are also tolerated under these hydrogenation conditions.

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