19495-08-0

Basic information

• Product Name: CINNAMOYL ISOTHIOCYANATE
• Synonyms: 3-PHENYLPROP-2-ENOYL ISOTHIOCYANATE;CINNAMOYL ISOTHIOCYANATE;Cinnamoyl isothiocyanate (Predominately trans);Cinmoyl isothiocyate
• CAS NO: 19495-08-0
• Molecular Formula: C₁₀H₇NOS
• Molecular Weight: 189.23
• Mol File: 19495-08-0.mol
• Article Data: 10

Chemical Properties

• Melting Point: 43-45°C
• Boiling Point: 311.9°Cat760mmHg
• Flash Point: 142.4°C
• Appearance: /
• Density: 1.07g/cm³
• Vapor Pressure: 0.000548mmHg at 25°C
• Refractive Index: 1.566
• CAS DataBase Reference: CINNAMOYL ISOTHIOCYANATE(CAS DataBase Reference)
• NIST Chemistry Reference: CINNAMOYL ISOTHIOCYANATE(19495-08-0)
• EPA Substance Registry System: CINNAMOYL ISOTHIOCYANATE(19495-08-0)

Safety Data

• HazardClass: IRRITANT-HARMFUL
• Hazardous Substances Data: 19495-08-0(Hazardous Substances Data)

Usage

General Description

Cinnamoyl isothiocyanate is a chemical compound derived from cinnamic acid and isothiocyanate. It is a member of the isothiocyanate family, which is known for its antibacterial and antifungal properties. Cinnamoyl isothiocyanate is found in plants such as cinnamon and horseradish, and is responsible for their pungent odor and taste. It has been studied for its potential use as a natural food preservative and antimicrobial agent. Additionally, it has shown promise in inhibiting the growth of certain cancer cells and may have potential as a therapeutic agent in the treatment of cancer and other diseases. However, further research is needed to fully understand its potential benefits and safety.

InChI:InChI=1/C10H7NOS/c12-10(11-8-13)7-6-9-4-2-1-3-5-9/h1-7H/b7-6+

Upstream product

• 540-72-7 sodium thiocyanide 
• 102-92-1 cinnamoyl chloride 
• 621-82-9 Cinnamic acid 
• 333-20-0 potassium thioacyanate 
• 1147550-11-5 ammonium thiocyanate 
• 345647-29-2 C₁₈H₂₈O₂Si 
• 345647-22-5 C₁₅H₂₂O₂Si 

Downstream Products

• 128992-93-8 O-isobutyl N-(3-phenylpropenoyl)thiocarbamate 
• 105197-50-0 C₁₄H₁₇NOS₂ 
• 5772-90-7 N-(4-methoxyphenyl)-N'-3-phenylpropenoylthiourea 
• 104291-41-0 N-cinnamoyl-N'-(4-nitrophenyl)thiourea 
• 77409-20-2 2-Diphenylamino-6-phenyl-5,6-dihydro-[1,3]thiazin-4-one 
• 76655-06-6 N-butyl-N'-(cinnamoyl)thiourea 
• 113283-13-9 O-(2-propenyl) N-(3-phenylpropenoyl)monothiocarbamate 
• 107399-75-7 1-(5-Oxo-4,5-dihydro-1H-pyrazol-3-yl)-3-[(E)-(3-phenyl-acryloyl)]-thiourea 
• 128992-95-0 O-trideuteriomethyl N-(3-phenylpropenoyl)thiocarbamate 
• 128992-90-5 O-propyl N-(3-phenylpropenoyl)thiocarbamate 
• 104291-49-8 7-styryltetrazolo<1,5-a><1,3,5>triazine-5(4H)-thione 
• 73924-32-0 1-Cinnamoyl-2-Thiobiuret 
• 53453-83-1 N-(5-bromomethyl-4,5-dihydro-thiazol-2-yl)-3-phenyl-acrylamide 
• 53453-85-3 N-(4,5-dihydro-thiazol-2-yl)-3-phenyl-acrylamide 

Relevant articles and documents

Design, synthesis, and bioassay of 4-thiazolinone derivatives as influenza neuraminidase inhibitors

A series of 4-thiazolinone derivatives (D1-D58) were designed and synthesized. All of the derivatives were evaluated in vitro for neuraminidase (NA) inhibitory activities against influenza virus A (H1N1), and the inhibitory activities of the five most pot

Pyrazolopyridine substituted 2,4-dichlorocinnamoyl thiourea compounds and application thereof

The invention discloses pyrazolopyridine substituted 2,4-dichlorocinnamoyl thiourea compounds and an application thereof as a plant growth regulator. As the plant growth regulator, the compounds can significantly increase the germination rate, promote rooting and cell division and effectively regulate plant growth.

Direct and facile synthesis of acyl isothiocyanates from carboxylic acids using trichloroisocyanuric acid/triphenylphosphine system

A mild, efficient, and practical method for one-step synthesis of alkanoyl and aroyl isothiocyanates from carboxylic acids using a safe and inexpensive mixed reagent, trichloroisocyanuric acid/triphenyl-phosphine is described at room temperature. Availability of the reagents and easy workup of the reaction make this method attractive for organic chemists.