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

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

Uses

Used in Food Industry:
Cinnamoyl isothiocyanate is used as a natural food preservative and antimicrobial agent for its ability to inhibit the growth of bacteria and fungi, thereby extending the shelf life of food products.
Used in Pharmaceutical Industry:
Cinnamoyl isothiocyanate is used as a potential therapeutic agent for its ability to inhibit the growth of certain cancer cells, suggesting its potential in the treatment of cancer and other diseases.
Used in Cosmetics Industry:
Cinnamoyl isothiocyanate may be used in cosmetics for its antimicrobial properties, helping to preserve the product and prevent the growth of harmful microorganisms.
Used in Agricultural Industry:
Cinnamoyl isothiocyanate can be used as a natural pesticide or fungicide in agriculture, helping to protect crops from bacterial and fungal infections.

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

Upstream product

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

Downstream Products

• 128992-90-5 O-propyl N-(3-phenylpropenoyl)thiocarbamate 
• 134773-16-3 1-Acetyl-3-[(E)-(3-phenyl-acryloyl)]-thiourea 
• 14598-03-9 6-phenylpropiorhodanine 
• 120189-50-6 6-phenyl-3-methylpropiorhodanine 
• 2757-10-0 N-methylcinnamamide 
• 556-61-6 methyl thioisocyanate 
• 128945-09-5 1-(4-Methoxyphenyl)-2-thioxo-4,5-bis[4-methoxyphenylimino]imidazolidin 
• 99006-77-6 (E)-1-{3-(4-Methoxy-phenyl)-4,5-bis-[(Z)-4-methoxy-phenylimino]-2-thioxo-imidazolidin-1-yl}-3-phenyl-propenone 
• 128945-06-2 1,3-Bis<4-methoxyphenyl>-2-cinnamoylimino-4,5-bis<4-methoxyphenylimino>imidazolidin 
• 77409-20-2 2-Diphenylamino-6-phenyl-5,6-dihydro-[1,3]thiazin-4-one 

Relevant articles and documents

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Pyrimidine-substituted cinnamyl thiourea compound and application thereof

The invention discloses a pyrimidine-substituted cinnamyl thiourea compound. The pyrimidine-substituted cinnamyl thiourea compound is shown as a formula I. The compound shown in the formula I is takenas a plant growth regulator. As proved by a wheat seed soaking experiment, the compound shown in the formula I can remarkably increase the wheat germinating rate, and remarkably promote rooting; as proved by an expanding test of cucumber cotyledon, the compound shown in the formula I remarkably promotes cell division, and can effectively regulate and control plant growth. The formula I is shown in the description.

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.

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

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HETEROCYCLIC DERIVATIVE HAVING INHIBITORY ACTIVITY ON TYPE-I 11 -HYDROXYSTEROID DEHYDROGENASE

Disclosed is a compound which is useful as an 11β-hydroxysteroid dehydrogenase type 1 inhibitor. A compound represented by the formula: its pharmaceutically acceptable salt, or a solvate thereof, wherein X is O or S, a broken line and a wavy line represent the presence or the absence of a bond, (i) when a broken line represents the presence of a bond, a wavy line represents the absence of a bond, R2 and R3 are each independently hydrogen, halogen, cyano, hydroxy, carboxy, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl or the like, (ii) when a broken line represents the absence of a bond, a wavy line represents the presence of a bond, R1 and R4 are each independently hydrogen, halogen or the like, R2 and R3 are each independently hydrogen, halogen, cyano, hydroxy, carboxy, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl or the like, and R5 and R6 are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl or the like.

Reaction of stable trialkylsilyl esters with Ph3P(SCN)2: A novel method for the preparation of acyl and aroyl isothiocyanates under neutral condition

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