16167-63-8

• 

• Basic information

  1. Product Name: 4-methoxybenzaldehyde N-(4-fluorophenyl)thiosemicarbazone
  2. Synonyms:
  3. CAS NO:16167-63-8
  4. Molecular Formula: C₁₅H₁₄FN₃OS
  5. Molecular Weight: 303.3546
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 16167-63-8.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 422.6°C at 760 mmHg
  3. Flash Point: 209.4°C
  4. Appearance: N/A
  5. Density: 1.22g/cm³
  6. Vapor Pressure: 2.39E-07mmHg at 25°C
  7. Refractive Index: 1.592
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 4-methoxybenzaldehyde N-(4-fluorophenyl)thiosemicarbazone(CAS DataBase Reference)
  11. NIST Chemistry Reference: 4-methoxybenzaldehyde N-(4-fluorophenyl)thiosemicarbazone(16167-63-8)
  12. EPA Substance Registry System: 4-methoxybenzaldehyde N-(4-fluorophenyl)thiosemicarbazone(16167-63-8)

• 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: 16167-63-8(Hazardous Substances Data)

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• Downstream Products
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• Hydrazinecarbothioamide,N-(4-fluorophenyl)-2-[(4-methoxyphenyl)methylene]-

  Cas No: 16167-63-8

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• Hydrazinecarbothioamide,N-(4-fluorophenyl)-2-[(4-methoxyphenyl)methylene]- cas 16167-63-8

  Cas No: 16167-63-8

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16167-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16167-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16167-63:
(7*1)+(6*6)+(5*1)+(4*6)+(3*7)+(2*6)+(1*3)=108
108 % 10 = 8
So 16167-63-8 is a valid CAS Registry Number.

16167-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-(4-fluorophenyl)-3-[(Z)-(4-methoxyphenyl)methylideneamino]thiourea

1.2 Other means of identification

Product number	-
Other names	4-methoxy-benzaldehyde 4-(4-fluoro-phenyl)-thiosemicarbazone

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:16167-63-8 SDS

16167-63-8Upstream product

• 330-94-9 4-(4-fluorophenyl)thiosemicarbazide 
• 123-11-5 4-methoxy-benzaldehyde 
• 1544-68-9 4-fluorophenyl isothiocyanate 

16167-63-8Downstream Products

• 16113-52-3 4-methoxy-benzaldehyde [3-(4-fluoro-phenyl)-5-methyl-4-oxo-thiazolidin-2-ylidene]-hydrazone 
• 16113-45-4 4-methoxy-benzaldehyde [3-(4-fluoro-phenyl)-4-oxo-thiazolidin-2-ylidene]-hydrazone 
• 16167-66-1 4-methoxy-benzaldehyde [5-ethyl-3-(4-fluoro-phenyl)-4-oxo-thiazolidin-2-ylidene]-hydrazone 
• 16113-60-3 4-methoxy-benzaldehyde [3-(4-fluoro-phenyl)-4-oxo-5-phenyl-thiazolidin-2-ylidene]-hydrazone 

16167-63-8Relevant articles and documents

Thio- and selenosemicarbazones as antiprotozoal agents against Trypanosoma cruzi and Trichomonas vaginalis

álvarez-Márquez, Manuel,Escario, José Antonio,Espinosa-Buitrago, Teresa,Fernández-Bola?os, José G.,Fonseca-Berzal, Cristina,Gómez-Barrio, Alicia,Gómez-Nú?ez, María,Ibá?ez-Escribano, Alexandra,López, óscar,Lacueva-Arnedo, Manuel,Martín-Pérez, Tania,Martínez-Montiel, Mónica,Merino-Montiel, Penélope,Montiel-Smith, Sara

, p. 781 - 791 (2022/03/09)

Herein, we report the preparation of a panel of Schiff bases analogues as antiprotozoal agents by modification of the stereoelectronic effects of the substituents on N-1 and N-4 and the nature of the chalcogen atom (S, Se). These compounds were evaluated towards Trypanosoma cruzi and Trichomonas vaginalis. Thiosemicarbazide 31 showed the best trypanocidal profile (epimastigotes), similar to benznidazole (BZ): IC50 (31)=28.72 μM (CL-B5 strain) and 33.65 μM (Y strain), IC50 (BZ)=25.31 μM (CL-B5) and 22.73 μM (Y); it lacked toxicity over mammalian cells (CC50 > 256 μM). Thiosemicarbazones 49, 51 and 63 showed remarkable trichomonacidal effects (IC50?=16.39, 14.84 and 14.89 μM) and no unspecific cytotoxicity towards Vero cells (CC50 ≥ 275 μM). Selenoisosters 74 and 75 presented a slightly enhanced activity (IC50=11.10 and 11.02 μM, respectively). Hydrogenosome membrane potential and structural changes were analysed to get more insight into the trichomonacidal mechanism.

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