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95037-35-7

2-(2,6-Dichloro-4-pyridyl)-2-propanol, also known as triclopyr, is a synthetic organic compound that functions as a systemic herbicide. It is specifically designed to control broadleaf weeds and woody plants, making it a valuable tool in various agricultural and forestry settings.
Used in Forestry:
Triclopyr is used as a herbicidal agent for controlling unwanted broadleaf weeds and woody plants in forestry applications. Its purpose is to maintain the health and growth of desired tree species by eliminating competing vegetation, thus ensuring a more productive and sustainable forest ecosystem.
Used in Pastures:
In pasture management, triclopyr is used as a selective herbicide to control broadleaf weeds. This application helps to improve the quality of forage for livestock, ensuring a healthier and more productive grazing environment.
Used in Non-Crop Areas:
Triclopyr is utilized as a herbicidal solution for managing unwanted vegetation in non-crop areas, such as roadsides, industrial sites, and recreational areas. Its use helps to maintain clear and safe spaces, as well as to control the spread of invasive plant species.
Used in Agricultural Settings:
Triclopyr is employed as a systemic herbicide in agricultural fields to control broadleaf weeds and woody plants that compete with crops for nutrients, water, and sunlight. This ensures optimal crop growth and yield, contributing to increased agricultural productivity.

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  • 95037-35-7 Structure

  • Basic information

    1. Product Name: 2-(2,6-Dichloro-4-pyridyl)-2-propanol
    2. Synonyms: 2-(2,6-Dichloro-4-pyridyl)-2-propanol;2-(2,6-Dichloropyridin-4-yl)propan-2-ol
    3. CAS NO:95037-35-7
    4. Molecular Formula: C8H9Cl2NO
    5. Molecular Weight: 206.06916
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95037-35-7.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-(2,6-Dichloro-4-pyridyl)-2-propanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,6-Dichloro-4-pyridyl)-2-propanol(95037-35-7)
    11. EPA Substance Registry System: 2-(2,6-Dichloro-4-pyridyl)-2-propanol(95037-35-7)

  • 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: 95037-35-7(Hazardous Substances Data)

95037-35-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95037-35-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,3 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95037-35:
(7*9)+(6*5)+(5*0)+(4*3)+(3*7)+(2*3)+(1*5)=137
137 % 10 = 7
So 95037-35-7 is a valid CAS Registry Number.

95037-35-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-Dichloro-4-pyridyl)-2-propanol

1.2 Other means of identification

Product number -
Other names 2-(2,6-Dichloro-4-pyridinyl)-2-propanol

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:95037-35-7 SDS

95037-35-7Downstream Products

95037-35-7Relevant articles and documents

ANTIVIRAL COMPOUNDS

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Paragraph 0730, (2015/03/13)

Disclosed herein are new antiviral compounds, together with pharmaceutical compositions that include one or more antiviral compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a paramyxovirus viral infection with one or more small molecule compounds. Examples of paramyxovirus infection include an infection caused by human respiratory syncytial virus (RSV).

Discovery of dual leucine zipper kinase (DLK, MAP3K12) inhibitors with activity in neurodegeneration models

Patel, Snahel,Cohen, Frederick,Dean, Brian J.,De La Torre, Kelly,Deshmukh, Gauri,Estrada, Anthony A.,Ghosh, Arundhati Sengupta,Gibbons, Paul,Gustafson, Amy,Huestis, Malcolm P.,Le Pichon, Claire E.,Lin, Han,Liu, Wendy,Liu, Xingrong,Liu, Yichin,Ly, Cuong Q.,Lyssikatos, Joseph P.,Ma, Changyou,Scearce-Levie, Kimberly,Shin, Young G.,Solanoy, Hilda,Stark, Kimberly L.,Wang, Jian,Wang, Bei,Zhao, Xianrui,Lewcock, Joseph W.,Siu, Michael

, p. 401 - 418 (2015/01/30)

Dual leucine zipper kinase (DLK, MAP3K12) was recently identified as an essential regulator of neuronal degeneration in multiple contexts. Here we describe the generation of potent and selective DLK inhibitors starting from a high-throughput screening hit. Using proposed hinge-binding interactions to infer a binding mode and specific design parameters to optimize for CNS druglike molecules, we came to focus on the di(pyridin-2-yl)amines because of their combination of desirable potency and good brain penetration following oral dosing. Our lead inhibitor GNE-3511 (26) displayed concentration-dependent protection of neurons from degeneration in vitro and demonstrated dose-dependent activity in two different animal models of disease. These results suggest that specific pharmacological inhibition of DLK may have therapeutic potential in multiple indications.

Substituted pyridyl compounds, herbicidal compositions and method of use

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, (2008/06/13)

Substituted pyridyl compounds, e.g. 2,6-dichloro-4(2-(2,2,2-trichloroethyl)oxiranyl) pyridine; herbicidal compositions containing such compounds and method for the control of undesired vegetation using these compositions.

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