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2-Amino-5-bromothiophenol is a chemical compound characterized by its molecular formula C6H6BrNS, a molecular weight of 200.09 g/mol, and a yellow solid appearance. It is known for its aromatic and sulfur-containing properties, making it a versatile and useful chemical in various research and industrial applications.

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  • 220301-84-8 Structure
  • Basic information

    1. Product Name: 2-aMino-5-broMothiophenol
    2. Synonyms: 2-Bromo-N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)-4-nitroaniline
    3. CAS NO:220301-84-8
    4. Molecular Formula: C6H6BrNS
    5. Molecular Weight: 204.08754
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220301-84-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-aMino-5-broMothiophenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-aMino-5-broMothiophenol(220301-84-8)
    11. EPA Substance Registry System: 2-aMino-5-broMothiophenol(220301-84-8)
  • 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: 220301-84-8(Hazardous Substances Data)

220301-84-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-Amino-5-bromothiophenol is utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.
Used in Dye and Pigment Production:
2-aMino-5-broMothiophenol is employed in the production of dyes and pigments, where its aromatic and sulfur-containing properties are leveraged to create a variety of colorants for different applications.
Used in Organic Synthesis:
2-Amino-5-bromothiophenol serves as a valuable building block in organic synthesis, enabling the creation of new compounds with relevant biological or industrial properties. Its potential applications in this field make it an important component in the development of novel chemical entities.
Used in Chemical and Industrial Processes:
Due to its aromatic nature and bromine substitution, 2-Amino-5-bromothiophenol plays a significant role in various chemical and industrial processes, where its unique properties are harnessed to achieve specific outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 220301-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,0 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 220301-84:
(8*2)+(7*2)+(6*0)+(5*3)+(4*0)+(3*1)+(2*8)+(1*4)=68
68 % 10 = 8
So 220301-84-8 is a valid CAS Registry Number.

220301-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-bromo-4-nitrophenyl)-4-chlorodithiazol-5-imine

1.2 Other means of identification

Product number -
Other names 2-Bromo-N-(4-chloro-5H-1,2,3-dithiazol-5-ylidene)-4-nitroaniline

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:220301-84-8 SDS

220301-84-8Relevant articles and documents

HETEROCYCLYLAMIDES AS GUT MICROSOMAL TRIGLYCERIDE TRANSPORT PROTEIN INHIBITORS

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Page/Page column 83, (2009/03/07)

Compounds represented by formula (I) are inhibitors of gut microsomal triglyceride transfer protein. Such compounds are useful in treating diseases or conditions such as diabetes and obesity, along with patients are risk for developing such diseases or conditions.

Discovery of benzothiazole derivatives as efficacious and enterocyte-specific MTP inhibitors

Vu, Chi B.,Milne, Jill C.,Carney, David P.,Song, Jeffrey,Choy, Wendy,Lambert, Philip D.,Gagne, David J.,Hirsch, Michael,Cote, Angela,Davis, Meghan,Lainez, Elden,Meade, Nekeya,Normington, Karl,Jirousek, Michael R.,Perni, Robert B.

scheme or table, p. 1416 - 1420 (2009/11/30)

A series of triamide derivatives bearing a benzothiazole core is shown to be potent microsomal triglyceride transfer protein (MTP) inhibitors. In order to minimize liver toxicity, these compounds have been optimized to have activity only in the enterocyte

GUT MICROSOMAL TRIGLYCERIDE TRANSPORT PROTEIN INHIBITORS

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Page/Page column 89-91, (2008/12/08)

Compounds represented by formula (I): are inhibitors of gut microsomal triglyceride transfer protein. Such compounds are useful in treating diseases or conditions such as diabetes and obesity, along with patients are risk for developing such diseases or conditions.

Novel 6-substituted benzothiazol-2-yl indolo[1,2-c]quinazolines and benzimidazo[1,2-c]quinazolines

Frère, Stéphane,Thiéry, Valérie,Bailly, Christian,Besson, Thierry

, p. 773 - 779 (2007/10/03)

The synthetic route to and a preliminary biological evaluation of novel indolo[1,2-c]quinazolines (8) and benzimidazo[1,2-c]quinazolines (9) are described. The products were obtained by condensation of the appropriate diamines (e.g. 2-(2-aminophenyl)indol

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