5980-23-4

Basic information

• Product Name: 3,5-DICHLOROBENZAMIDE
• Synonyms: 3,5-DICHLOROBENZAMIDE;3,5-DICHLOROBENZAMIDE 99%
• CAS NO: 5980-23-4
• Molecular Formula: C₇H₅Cl₂NO
• Molecular Weight: 190.03
• Product Categories: Anilines, Amides & Amines;Chlorine Compounds
• Mol File: 5980-23-4.mol
• Article Data: 7

Chemical Properties

• Melting Point: 160 °C
• Boiling Point: 264.2 °C at 760 mmHg
• Flash Point: 113.6 °C
• Appearance: /
• Density: 1.439 g/cm³
• Vapor Pressure: 0.00984mmHg at 25°C
• Refractive Index: 1.596
• PKA: 14.82±0.50(Predicted)
• BRN: 2249768
• CAS DataBase Reference: 3,5-DICHLOROBENZAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DICHLOROBENZAMIDE(5980-23-4)
• EPA Substance Registry System: 3,5-DICHLOROBENZAMIDE(5980-23-4)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 22-24/25
• Hazardous Substances Data: 5980-23-4(Hazardous Substances Data)

Usage

General Description

3,5-Dichlorobenzamide is a chemical compound with the molecular formula C7H5Cl2NO. It is a white crystalline solid that is soluble in organic solvents and slightly soluble in water. 3,5-Dichlorobenzamide is primarily used as an intermediate in the production of pharmaceuticals and agricultural chemicals. It is also known to inhibit the growth of microorganisms, making it useful in the formulation of disinfectant and antimicrobial products. However, it is important to handle 3,5-Dichlorobenzamide with care as it is considered to be toxic if ingested or inhaled, and can cause skin and eye irritation upon contact. Overall, 3,5-Dichlorobenzamide is a versatile compound with various industrial applications and should be used with caution due to its potential hazards.

InChI:InChI=1/C7H5Cl2NO/c8-5-1-4(7(10)11)2-6(9)3-5/h1-3H,(H2,10,11)

Upstream product

• 6575-00-4 3,5-dichlorobenzonitrile 
• 64-18-6 formic acid 
• 541-73-1 1,3-Dichlorobenzene 
• 100-51-6 benzyl alcohol 
• 60211-57-6 3,5-dichlorobenzyl alcohol 
• 51-36-5 3,5-dichlorobenzoic acid 

Downstream Products

• 626-43-7 3,5-Dichloroaniline 
• 104417-83-6 3,5-dichlorobenzoyl isocyanate 
• 403509-13-7 N-[1-(1H-1,2,3-benzotriazol-1-yl)-2,2-dichloropropyl]-3,5-dichlorobenzamide 
• 124808-45-3 (3,5-Dichloro-benzoyl)-carbamic acid (1R,3R,5S)-8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl ester 
• 945257-74-9 3,5-dichloro-N-{4-[(5,5-dimethyl-2,4-dioxo-3-{4-[(trifluoro-methyl)thio]phenyl}imidazolidin-1-yl)methyl]pyridin-2-yl}benzamide 
• 25217-43-0 methyl (3,5-dichlorophenyl)carbamate 
• 53882-15-8 3,5-diaminobenzamide 

Relevant articles and documents

Visible light-mediated synthesis of amides from carboxylic acids and amine-boranes

Here, a photocatalytic deoxygenative amidation protocol using readily available amine-boranes and carboxylic acids is described. This approach features mild conditions, moderate-to-good yields, easy scale-up, and up to 62 examples of functionalized amides with diverse substituents. The synthetic robustness of this method was also demonstrated by its application in the late-stage functionalization of several pharmaceutical molecules.

Atomically Dispersed Ru on Manganese Oxide Catalyst Boosts Oxidative Cyanation

There is a strong incentive for environmentally benign and sustainable production of organic nitriles to avoid the use of toxic cyanides. Here we report that manganese oxide nanorod-supported single-site Ru catalysts are active, selective, and stable for oxidative cyanation of various alcohols to give the corresponding nitriles with molecular oxygen and ammonia as the reactants. The very low amount of Ru (0.1 wt %) with atomic dispersion boosts the catalytic performance of manganese oxides. Experimental and theoretical results show how the Ru sites enhance the ammonia resistance of the catalyst, bolstering its performance in alcohol dehydrogenation and oxygen activation, the key steps in the oxidative cyanation. This investigation demonstrates the high efficiency of a single-site Ru catalyst for nitrile production.

Tetrazole urease inhibitor type feed additive and preparation method thereof

The invention discloses a tetrazole urease inhibitor type feed additive and a preparation method thereof and belongs to the technical field of synthesis of feed additives. According to the technical scheme, a structural formula of the tetrazole urease inhibitor type feed additive is shown in the description. The invention further discloses the preparation method of the tetrazole urease inhibitor type feed additive. The tetrazole urease inhibitor type feed additive prepared by the preparation method can be used as non-protein nitrogen and has a certain inhibition effect on urease; the tetrazoleurease inhibitor type feed additive has the effects of sterilizing and resisting ulcer and has a potential of being used as an excellent animal feed additive.