101337-92-2

• 

• Basic information

  1. Product Name: 6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL
  2. Synonyms: 5-CHLORO-6-FLUOROBENZIMIDAZOLE-2-THIOLE;BUTTPARK 81\03-18;6-Chloro-5-fluorobenzimidazole-2-thiole;6-chloro-5-fluoro-2-mercaptobenzimidazole;2-Benzothiazolamine,5-chloro-6-fluoro-(9CI);TIMTEC-BB SBB003521;6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL;6-CHLORO-5-FLUORO-1H-BENZO[D]IMIDAZOLE-2-THIOL
  3. CAS NO:101337-92-2
  4. Molecular Formula: C₇H₄ClFN₂S
  5. Molecular Weight: 202.64
  6. EINECS: N/A
  7. Product Categories: BENZOTHIAZOLE
  8. Mol File: 101337-92-2.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: 298～301℃
  2. Boiling Point: 350.6±45.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.625±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 3.27±0.10(Predicted)
  10. CAS DataBase Reference: 6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL(CAS DataBase Reference)
  11. NIST Chemistry Reference: 6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL(101337-92-2)
  12. EPA Substance Registry System: 6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL(101337-92-2)

• 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: 101337-92-2(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 4-AMINOBENZOYLHYDRAZIDE

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• 2-Benzothiazolamine,5-chloro-6-fluoro-

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• 2-Benzothiazolamine,5-chloro-6-fluoro-

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• Zibo Hangyu Biotechnology Development Co., Ltd
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• 2-Benzothiazolamine,5-chloro-6-fluoro-

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• 2-BENZOTHIAZOLAMINE,5-CHLORO-6-FLUORO-

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101337-92-2 Usage

General Description

6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL is a chemical compound with the molecular formula C7H4ClFN2S. It is a benzimidazole derivative with a chlorine atom at the 6 position and a fluorine atom at the 5 position. 6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL belongs to the class of thiazoles and has a thiol group at the 2 position. It is used in the pharmaceutical industry for the synthesis of various medications and has potential applications in the field of medicinal chemistry. Additionally, it may have biological activities such as antimicrobial and antifungal properties due to its structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 101337-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,3 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101337-92:
(8*1)+(7*0)+(6*1)+(5*3)+(4*3)+(3*7)+(2*9)+(1*2)=82
82 % 10 = 2
So 101337-92-2 is a valid CAS Registry Number.

101337-92-2SDS

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	6-CHLORO-5-FLUOROBENZIMIDAZOLE-2-THIOL

1.2 Other means of identification

Product number	-
Other names	BUTTPARK 81 3-18

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:101337-92-2 SDS

101337-92-2Upstream product

• 367-21-5 3-chloro-4-fluorophenylamine 
• 333-20-0 potassium thioacyanate 
• 154371-25-2 1-(3-chloro-4-fluorophenyl)thiourea 

101337-92-2Downstream Products

• 142335-07-7 2-amino-5-chloro-6-fluorophenyl disulfide 
• 1251838-06-8 N-(5-chloro-6-fluoro-1,3-benzothiazol-2-yl)-1,1'-biphenyl-4-carboxamide 
• 1416210-02-0 C₂₁H₁₂ClFN₂O₂S 
• 1416209-97-6 C₁₇H₁₂ClFN₂O₂S 
• 1378508-72-5 6-chloro-7-fluoro-2-phenyl-2H-1,4-benzothiazin-3(4H)-one 
• 1378508-65-6 6-chloro-7-fluoro-3-phenyl-3,4-dihydro-2H-1,4-benzothiazine 
• 1373398-74-3 2-chloro-N-(5-chloro-6-fluorobenzothiazol-2yl)acetamide 
• 1304134-19-7 C₁₉H₁₅ClFN₃O₃S 
• 1304134-18-6 C₂₀H₁₇ClFN₃O₃S 
• 1304134-17-5 C₁₉H₁₅ClFN₃O₂S 
• 1304134-21-1 C₂₀H₁₇ClFN₃O₄S 
• 1304134-20-0 C₂₁H₂₀ClFN₄O₂S 
• 1304134-22-2 C₁₉H₁₄ClFN₄O₄S 
• 1304134-23-3 C₁₉H₁₄ClFN₄O₄S 

101337-92-2Relevant articles and documents

Synthesis and antifungal activity against strains of Candida albicans of 6-fluoro-4(5 or 7)-chloro-2-(difluorobenzoyl)aminobenzothiazoles

Armenise, Domenico,De Laurentis, Nicolino,Reho, Antonia,Rosato, Antonio,Morlacchi, Flaviano

, p. 771 - 775 (2004)

A series of 6-fluoro-4-(5 or 7)-chloro-2-(difluorobenzoyl) aminobenzothiazoles 3a-r were prepared to investigate their potential biological activity. In this work, the results of their in vitro antifungal activity against some strains of Candida albicans

Synthesis, anti-inflammatory, analgesic, 5-lipoxygenase (5-LOX) inhibition activities, and molecular docking study of 7-substituted coumarin derivatives

Srivastava, Pavan,Vyas, Vivek K.,Variya, Bhavesh,Patel, Palak,Qureshi, Gulamnizami,Ghate, Manjunath

supporting information, p. 130 - 138 (2016/07/11)

In the present study, 7-subsituted coumarin derivatives were synthesized using various aromatic and heterocyclic amines, and evaluated in vivo for anti-inflammatory and analgesic activity, and for ulcerogenic risk. The most active compounds were evaluated in vitro for 5-lipoxygenase (5-LOX) inhibition. Docking study was performed to predict the binding affinity, and orientation at the active site of the enzyme. In vivo anti-inflammatory and analgesic activity, and in vitro 5-LOX enzyme inhibition study revealed that compound 33 and 35 are the most potent compounds in all the screening methods. In vitro kinetic study of 35 showed mixed or non-competitive type of inhibition with 5-LOX enzyme. Presence of [Formula presented]3 group in 35 and [Formula presented] in 33 at C6-position of benzothiazole ring were found very important substitutions for potent activity.

Synthesis and biological activity of 2-amino-4H-pyrimido[2,1-b][1,3] benzothiazole-3-carboxylates

Chaithanya,Vaidya,Nagendrappa

experimental part, p. 1618 - 1620 (2012/01/05)

3-Chloro-4-fluoro aniline (1) on reaction with potassium thiocyanate (2) followed by the addition of bromine in acetic acid medium yielded 2-amino 5-chloro-6-fluro[2,1-b][1,3]benzothiazole (3). Compound 3 when treated with β-cyanoester undergoes cycloaddi

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