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100648-13-3

Triclabendazole sulfoxide is a metabolite of Triclabendazole, an anthelmintic drug that is effective against various stages of fluke, including immature, mature, and adult forms.

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  • 1H-Benzimidazole,6-chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-

    Cas No: 100648-13-3

  • USD $ 1.9-2.9 / Gram

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  • 100648-13-3 Structure

  • Basic information

    1. Product Name: Triclabendazole sulfoxide
    2. Synonyms: TRICLABENDAZOLE SULFOXIDE;6-chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1h-benzimidazole;triclabendazole sulfoxide:6-chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1h-benzIMIDAZOLE;6-chloro-5-(2,3-dichlorophenoxy)-2-(methylsulfinyl)-1H-benzo[d]imidazole
    3. CAS NO:100648-13-3
    4. Molecular Formula: C14H9Cl3N2O2S
    5. Molecular Weight: 375.65746
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100648-13-3.mol

  • Chemical Properties

    1. Melting Point: approximate 189℃ (dec.)
    2. Boiling Point: 547.6 °C at 760 mmHg
    3. Flash Point: 285 °C
    4. Appearance: /
    5. Density: 1.69
    6. Vapor Pressure: 4.81E-12mmHg at 25°C
    7. Refractive Index: 1.749
    8. Storage Temp.: Refrigerator
    9. Solubility: Acetonitrile (Slightly), Methanol (Slightly)
    10. BRN: 5829656
    11. CAS DataBase Reference: Triclabendazole sulfoxide(CAS DataBase Reference)
    12. NIST Chemistry Reference: Triclabendazole sulfoxide(100648-13-3)
    13. EPA Substance Registry System: Triclabendazole sulfoxide(100648-13-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 100648-13-3(Hazardous Substances Data)

100648-13-3 Usage

Uses

Used in Pharmaceutical Industry:
Triclabendazole sulfoxide is used as an anthelmintic agent for the treatment of fluke infections. It is effective against all stages of the fluke, making it a valuable tool in combating this parasitic disease.

Check Digit Verification of cas no

The CAS Registry Mumber 100648-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,4 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100648-13:
(8*1)+(7*0)+(6*0)+(5*6)+(4*4)+(3*8)+(2*1)+(1*3)=83
83 % 10 = 3
So 100648-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Cl3N2O2S/c1-22(20)14-18-9-5-8(16)12(6-10(9)19-14)21-11-4-2-3-7(15)13(11)17/h2-6H,1H3,(H,18,19)

100648-13-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (35391)  Triclabendazole sulfoxide  VETRANAL™, analytical standard

  • 100648-13-3

  • 35391-10MG

  • 1,621.62CNY

  • Detail

100648-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-5-(2,3-dichlorophenoxy)-2-methylsulfinyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names Tcbz-SX

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:100648-13-3 SDS

100648-13-3Upstream product

100648-13-3Downstream Products

100648-13-3Relevant articles and documents

2H-Benzimidazoles (Isobenzimidazoles). Part 7. A New Route to Triclabendazole and Congeneric Benzimidazoles

Iddon, Brian,Kutschy, Peter,Robinson, Andrew G.,Suschitzky, Hans,Kramer, Walter,Neugebauer, Franz A.

, p. 3129 - 3134 (2007/10/02)

A new synthesis of the selective anthelmintic agent triclabendazole 7 from the readily available 5,6-dichloro-2H-benzimidazole-2-spirocyclohexane 2 by simple steps is described.Analogous benzimidazoles difficult to prepare by conventional methods are similarly obtained.Triclabendazole can exist as a low-melting metastable solid (m.p. 85-90 deg C) convertible by heating or recrystallisation from ethanol into its stable form (m.p. 176-178 deg C).

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