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2,6-Dichlorophenol acetate, with the chemical formula C8H6Cl2O3, is a chemical compound characterized by a phenolic ring with two chlorine atoms and an acetate group. It is recognized for its herbicidal and plant growth regulatory properties, which function by disrupting plant hormones and inhibiting plant growth. Classified as a hazardous substance, 2,6-dichlorophenol acetate requires careful handling and proper disposal to prevent environmental contamination and health risks.

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  • 28165-71-1 Structure
  • Basic information

    1. Product Name: 2,6-DICHLOROPHENOL ACETATE
    2. Synonyms: Acetic acid, 2,6-dichlorophenyl ester;2,6-DICHLOROPHENOL ACETATE;Phenol, 2,6-dichloro-, acetate;2,6-Dichlorophenyl acetate
    3. CAS NO:28165-71-1
    4. Molecular Formula: C8H6Cl2O2
    5. Molecular Weight: 205.04
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28165-71-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.9°Cat760mmHg
    3. Flash Point: 115.4°C
    4. Appearance: /
    5. Density: 1.358g/cm3
    6. Vapor Pressure: 0.00748mmHg at 25°C
    7. Refractive Index: 1.54
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,6-DICHLOROPHENOL ACETATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,6-DICHLOROPHENOL ACETATE(28165-71-1)
    12. EPA Substance Registry System: 2,6-DICHLOROPHENOL ACETATE(28165-71-1)
  • 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: 28165-71-1(Hazardous Substances Data)

28165-71-1 Usage

Uses

Used in Agricultural Industry:
2,6-Dichlorophenol acetate is used as a herbicide for controlling the growth of unwanted plants. It targets the hormonal balance in plants, leading to their growth inhibition and eventual death, thus providing a means to manage and protect crops from invasive species.
Used in Plant Growth Regulation:
In the field of horticulture and plant cultivation, 2,6-dichlorophenol acetate is used as a plant growth regulator. It can manipulate the growth patterns of plants, which is beneficial for specific agricultural practices where controlled growth is desired.

Check Digit Verification of cas no

The CAS Registry Mumber 28165-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,6 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28165-71:
(7*2)+(6*8)+(5*1)+(4*6)+(3*5)+(2*7)+(1*1)=121
121 % 10 = 1
So 28165-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Cl2O2/c1-5(11)12-8-6(9)3-2-4-7(8)10/h2-4H,1H3

28165-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-DICHLOROPHENOL ACETATE

1.2 Other means of identification

Product number -
Other names 2,6-Dichlorophenyl acetate

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:28165-71-1 SDS

28165-71-1Relevant articles and documents

Development of pH-activatable fluorescent probes for rapid visualization of metastatic tumours and fluorescence-guided surgeryviatopical spraying

Cao, Wenwen,Li, Xiaoxin,Wu, Peng,Xiong, Hu

supporting information, p. 10636 - 10639 (2021/10/19)

A series of pH-activatable aza-BODIPY-based fluorescent probes were developed for rapid cancer visualization and real-time fluorescence-guided surgery by harnessing topical spraying. These probes exhibited good water-solubility, a tunable pKafrom 5.0 to 7.9, and stable intense NIR emission at ~725 nm under acidic conditions.AzaB5with a pKavalue of 6.7 was able to rapidly and clearly visualize pulmonary and abdominal metastatic tumours including tiny metastases less than 2 mmviatopical spraying, further improving intraoperative fluorescence-guided resection. We believe thatAzaB5is promising as a powerful tool to rapidly delineate a broad range of malignancies and assist surgical tumour resection.

A general strategy to optimize the performance of aza-BODIPY-based probes for enhanced photoacoustic properties

Yadav, Anuj K.,Tapia Hernandez, Rodrigo,Chan, Jefferson

, p. 415 - 441 (2021/07/26)

In this chapter, we describe a generalizable strategy to obtain a high PA output platform that is optimized for ratiometric imaging. Our approach entails conformationally restricting pendant aryl rings on the aza-BODIPY core to enhance orbital overlap which consequently increases the extinction coefficient. This strategy can potentially be applied to other dye platforms to enhance their signal intensity. We provide detailed protocols for the synthesis, in vitro characterization, and in vivo application.

BETA-HYDROXYETHYLAMINES FOR USE IN THE TREATMENT OR PREVENTION OF NON-ALCOHOLIC FATTY LIVER DISEASES

-

Page/Page column 59; 60, (2019/04/11)

There is herein provided a compound of formula (I) or a pharmaceutically acceptable salt thereof, for use in the treatment of a non-alcoholic fatty liver disease (NAFLD), such as non-alcoholic steatohepatitis (NASH), wherein X, R1, R2, R3 and n have meanings as provided in the description.

A Conformationally Restricted Aza-BODIPY Platform for Stimulus-Responsive Probes with Enhanced Photoacoustic Properties

Zhou, Effie Y.,Knox, Hailey J.,Liu, Chang,Zhao, Weili,Chan, Jefferson

supporting information, p. 17601 - 17609 (2019/11/11)

Photoacoustic (PA) dyes, which absorb near-infrared (NIR) light to generate an ultrasonic signal, can be detected at centimeter depths in tissues with significantly higher resolution than dyes imaged with fluorescence-based methods. As such, PA agents show great promise as research tools for the study of live-animal disease models. However, the development of activatable PA probes has been hampered by the relative scarcity of appropriate PA-active molecular platforms with properties that can be manipulated in a rational manner. Herein we synthesized and evaluated six modifications to the aza-BODIPY dye platform with respect to their absorbance, fluorescence, and PA properties. We identified a promising conformationally restricted aza-BODIPY (CRaB) scaffold that prioritizes three criteria necessary for the design of stimulus-responsive dyes with optimal ratiometric PA response: absorbance at NIR wavelengths, strong PA intensity, and large Δλ upon interaction with the desired stimulus. Using this scaffold, we synthesized three chemically diverse stimulus-responsive PA probes and demonstrated between 2- and 8-fold improvements in theoretical ratiometric response in vitro. This suggests that improvements in PA parameters are generalizable. Finally, we validated the in vitro turnover of each CRaB PA probe and demonstrated the in vivo potential of the CRaB scaffold by direct comparison to an established hypoxia-responsive probe for the detection of tumor hypoxia.

Werner transition-metal complex (WTMC)-mediated mild and efficient chemo-selective acylation of phenols and anilines under solvent-free condition

Sarief, Abdulla,Haque, SK Manirul,Feroze, Syed Mudabbir,Arifuddin, Mohammed

, p. 1104 - 1109 (2018/09/27)

Werner-type transition-metal complexes (WTMC) such as [Co(NH3)5Cl]Cl2, Cu[(NH3)4]SO4, Mn(acac)3, Ni[(NH3)6]Cl2, Ni[(en)3]S2O3, and Hg[Co(SCN)4] efficiently promote the chemoselective acetylation of phenols and anilines under solvent-free condition. The results of this study clearly shows that the optimal condition for the acetylation of anilines/phenols (1 mmol) (2a–r) with acetic anhydride (1.2 mmol) in the presence of WTMC (1 mmol) and two drops of H3PO4 on heating for 10 min under solvent-free condition gives the corresponding acetanilides/phenyl acetate (3a–r) in good to excellent yield. Furthermore, the method is simple, efficient, chemoselective, and eco-friendly under solvent-free condition for the acetylation of anilines and phenols promoted by WTMC by using acetic anhydrate as the acetylating agent. The simple preparation of the catalyst, easy procedure of the acetylation reaction, and simple work-up indicate the importance of WTMC for such reactions.

COMPOUNDS FOR THE TREATMENT OF HYPERGLYCAEMIA

-

Page/Page column 62; 63, (2017/09/28)

There is herein provided a compound of formula (I) or a pharmaceutically acceptable salt thereof, for use in the treatment of hyperglycaemia or a disorder characterized by hyperglycaemia, such as type 2 diabetes, wherein X, R1, R2, R3 and n have meanings as provided in the description.

Photoacoustic Probes for Ratiometric Imaging of Copper(II)

Li, Hao,Zhang, Pamela,Smaga, Lukas P.,Hoffman, Ryan A.,Chan, Jefferson

supporting information, p. 15628 - 15631 (2016/01/09)

Photoacoustic tomography has emerged as a promising alternative to MRI and X-ray scans in the clinical setting due to its ability to afford high-resolution images at depths in the cm range. However, its utility has not been established in the basic research arena owing to a lack of analyte-specific photoacoustic probes. To this end, we have developed acoustogenic probes for copper(II)-1 and -2 (APC-1 and APC-2, a water-soluble congener) for the chemoselective visualization of Cu(II), a metal ion which plays a crucial role in chronic neurological disorders such as Alzheimer's disease. To detect Cu(II), we have equipped both APCs with a 2-picolinic ester sensing module that is readily hydrolyzed in the presence of Cu(II) but not by other divalent metal ions. Additionally, we designed APC-1 and APC-2 explicitly for ratiometric photoacoustic imaging by using an aza-BODIPY dye scaffold exhibiting two spectrally resolved NIR absorbance bands which correspond to the 2-picolinic ester capped and uncapped phenoxide forms. The normalized ratiometric turn-on responses for APC-1 and APC-2 were 89- and 101-fold, respectively.

The first vinyl acetate mediated organocatalytic transesterification of phenols: A step towards sustainability

Kumar, Manoj,Bagchi, Sourav,Sharma, Anuj

supporting information, p. 8329 - 8336 (2015/11/10)

The present report outlines our efforts toward a simple yet elegant protocol for O-acylation of a wide variety of phenols. This highly enabling and solventless method relies on vinyl acetate as an innocuous acyl donor and DABCO as an organocatalyst. Operational simplicity, excellent yields, higher and faster conversion rates without excess reagents, a simple workup and essentially no need of columns are some of the salient features of the reported protocol.

O-acylation of substituted phenols with various alkanoyl chlorides under phase-transfer catalyst conditions

Simion, Alina Marieta,Hashimoto, Iwao,Mitoma, Yoshiharu,Egashira, Naoyoshi,Simion, Cristian

experimental part, p. 921 - 931 (2012/02/01)

Esterification of several types of mono-and disubstituted phenols with various mono-and dialkanoyl chlorides was performed in phase-transfer catalysis conditions, using tetrabutylammonium chloride in a mixture of aqueous NaOH and dichloromethane. The process is particularly efficient (almost quantitative yields) as well as rapid (only 5 min reaction time, at a temperature of0°C). Taylor & Francis Group, LLC.

Highly efficient dynamic kinetic resolution of secondary aromatic alcohols with low-cost and easily available acid resins as racemization catalysts

Cheng, Yongmei,Xu, Gang,Wu, Jianping,Zhang, Chensheng,Yang, Lirong

supporting information; experimental part, p. 2366 - 2369 (2010/06/13)

A new and efficient dynamic kinetic resolution (DKR) process of secondary aromatic alcohols was developed with acid resins as racemization catalysts. Acid resin CD8604 was shown to have excellent racemization activity and good biocompatibility. When employing CD8604 and complex acyl donors as racemization catalyst and acyl donor, respectively, enantiomerically pure aromatic acetate was obtained with excellent yield and ee values through the DKR process. It is noteworthy that the system could be reused more than 10 times with little loss of yield and ee value.

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