126833-17-8

Basic information

• Product Name: FENHEXAMID
• Synonyms: Cyclohexanecarboxamide, N-(2,3-dichloro-4-hydroxyphenyl)-1-methyl-;FENHEXAMID STANDARD;fenhexamid N-(2,3-dichlor-4-hydroxyphenyl)-1-methylcyclohexancarboxamid;Fenhexamid 250mg [126833-17-8];Decree;Elevate;KBR 2738;Teldor
• CAS NO: 126833-17-8
• Molecular Formula: C14H17Cl2NO2
• Molecular Weight: 302.2
• EINECS: 422-530-5
• Product Categories: Agro-Products;Amines;Aromatics
• Mol File: 126833-17-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 141°
• Boiling Point: 320°C(lit.)
• Flash Point: 150 °C
• Appearance: /
• Density: 1.338g/cm³
• Vapor Pressure: 5.26E-09mmHg at 25°C
• Refractive Index: 1.604
• Storage Temp.: 0-6°C
• PKA: 7.73±0.36(Predicted)
• Merck: 14,3974
• BRN: 8996658
• CAS DataBase Reference: FENHEXAMID(CAS DataBase Reference)
• NIST Chemistry Reference: FENHEXAMID(126833-17-8)
• EPA Substance Registry System: FENHEXAMID(126833-17-8)

Safety Data

• Hazard Codes: N
• Statements: 51/53
• Safety Statements: 61
• RIDADR: UN 3077 9/PG 3
• WGK Germany: 2
• RTECS: GU7879550
• HazardClass: 9
• PackingGroup: III
• Hazardous Substances Data: 126833-17-8(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 126833-17-8 differently. You can refer to the following data:
1. Hydroxyanilide fungicide.
2. Fungicide.

Definition

ChEBI: An aromatic amide resulting from the formal condensation of the carboxy group of 1-methylcyclohexanecarboxylic acid with the amino group of 4-amino-2,3-dichlorophenol.

Hazard

Low toxicity by ingestion, inhalation, and skin contact.

Agricultural Uses

Fungicide: Fungicide; for control of Botrytis cinerea and related diseases on Rubus, Ribes, bushberries, caneberries, grapes, pistachios, strawberries, ornamentals and other crops. Control of Monilinia diseases of almonds and stone fruit. On grapes and grapevines for suppression of powdery mildew and to control bunch rot[83].

Trade name

KBR-2738

InChI:InChI=1/C14H17Cl2NO2/c1-14(7-3-2-4-8-14)13(19)17-9-5-6-10(18)12(16)11(9)15/h5-6,18H,2-4,7-8H2,1H3,(H,17,19)

Upstream product

• 2890-61-1 1-methyl-1-cyclohexancarboxylic acid chloride 
• 39183-17-0 4-hydroxy-2,3-dichloroaniline 
• 576-24-9 2,3-dichlorophenol 
• 201656-71-5 2,3-dichloro-4-(2-phenyldiazen-1-yl)phenol 
• 201230-82-2 carbon monoxide 
• 1192-37-6 methylenecyclohexane 

Related news

Toxic responses and antioxidative enzymes activity of Scenedesmus obliquus exposed to FENHEXAMID (cas 126833-17-8) and atrazine, alone and in mixture07/30/2019

Laboratory studies were conducted to determine the effects of different concentrations of fenhexamid and atrazine (25, 50 and 100 µg L−1) on growth and oxidative stress on Scenedesmus obliquus (microalgae) after exposure for 24, 48, and 96 h. In addition, residues of fenhexamid and atrazine wer...detailed

Residual pattern of FENHEXAMID (cas 126833-17-8) on pepper fruits grown under greenhouse conditions using HPLC and confirmation via tandem mass spectrometry07/29/2019

Fenhexamid (25%, SC) was sprayed on pepper fruits grown under greenhouse conditions at the recommended dose rate of 20 g/20 L water. Fruit samples were collected randomly at 0 (2 h after application), 1, 2, 4, 6, 8, 11, and 14 days post-application. The samples were extracted with acetonitrile, ...detailed

Evaluation of the effect of FENHEXAMID (cas 126833-17-8) and mepanipyrim in the volatile composition of Tempranillo and Graciano wines07/27/2019

Grapes from Vitis vinifera var. Tempranillo and Graciano of La Rioja (North Central Spain) were vinified after addition of two fungicides (mepanipyrim and fenhexamid) at concentrations corresponding to their MRLs. These fungicides are commonly used in the vine growing to control botrytis disease...detailed

Effect of FENHEXAMID (cas 126833-17-8) and cyprodinil on the expression of cell cycle- and metastasis-related genes via an estrogen receptor-dependent pathway in cellular and xenografted ovarian cancer models07/25/2019

ABSTRACTFenhexamid and cyprodinil are antifungal agents (pesticides) used for agriculture, and are present at measurable amounts in fruits and vegetables. In the current study, the effects of fenhexamid and cyprodinil on cancer cell proliferation and metastasis were examined. Additionally, the p...detailed

Efficacy of FENHEXAMID (cas 126833-17-8) treatments against Botrytis cinerea in grapevine as affected by time of application and meteorological conditions07/23/2019

Grape bunch rot caused by Botrytis cinerea is one of the major fungal diseases of grapevine (Vitis vinifera L.) worldwide. Besides crop cultural measures, botryticides are used on a regular basis for controlling bunch rot. To investigate the impact of (i) the time of application and (ii) the met...detailed

Baseline sensitivity of Monilinia laxa from Greece to FENHEXAMID (cas 126833-17-8) and analysis of FENHEXAMID (cas 126833-17-8)-resistant mutants07/22/2019

Fenhexamid is a hydroxyanilide fungicide with excellent performance against Botrytis cinerea but also effective against Monilinia spp. which cause brown rot disease in apple and stone fruit. A total of 75 Monilinia laxa field isolates were utilized to determine baseline sensitivity while a numbe...detailed

Relevant articles and documents

Palladium-Catalyzed Markovnikov Hydroaminocarbonylation of 1,1-Disubstituted and 1,1,2-Trisubstituted Alkenes for Formation of Amides with Quaternary Carbon

Hydroaminocarbonylation of alkenes is one of the most promising yet challenging methods for the synthesis of amides. Herein, we reported the development of a novel and effective Pd-catalyzed Markovnikov hydroaminocarbonylation of 1,1-disubstituted or 1,1,2-trisubstituted alkenes with aniline hydrochloride salts to afford amides bearing an α quaternary carbon. The reaction makes use of readily available starting materials, tolerates a wide range of functional groups, and provides a facile and straightforward approach to a diverse array of amides bearing an α quaternary carbon. Mechanistic investigations suggested that the reaction proceeded through a palladium hydride pathway. The hydropalladation and CO insertion are reversible, and the aminolysis is probably the rate-limiting step.

Synergistic Combinations Of Active Ingredients

The present invention relates to novel active compound combinations comprising, firstly, at least one known compound of the formula (I) in which R1 and A have the meanings given in the description and, secondly, at least one further known active compound from groups (2) to (27) listed in the description, which combinations are highly suitable for controlling animal pests such as insects and unwanted acarids and also phytopathogenic fungi.

Fungicidal combinations of active substances

The novel active compound combinations of a fluoro-benzothiazole derivative of the formula and the active compound groups (1) to (51) listed in the description have very good fungicidal properties.