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2-Amino-6- trifluoromethylbenzothiazole

2-Amino-6- trifluoromethylbenzothiazole

Product Details:

  • Shape Crystalline
  • HS Code 29349900
  • Melting Point 126-130 C
  • Ingredients 2-Amino-6-trifluoromethylbenzothiazole
  • Physical Form Powder
  • Application Research chemical; Intermediate for pharmaceuticals, agrochemicals, and specialty chemicals
  • Appearance Off-white to pale yellow powder
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2-Amino-6- trifluoromethylbenzothiazole Price And Quantity

  • 1 Number

2-Amino-6- trifluoromethylbenzothiazole Product Specifications

  • Analytical Grade; Industrial Grade
  • High chemical stability; Electronegative trifluoromethyl group; Reacts with electrophiles and nucleophiles
  • 8-image as per chemical structure; refer to CAS 74650-86-99
  • May be harmful if swallowed. Handle with care.
  • 777-12-8
  • Pharmaceutical Intermediate; Organic Chemical
  • Characteristic benzothiazole-like odor
  • Used in synthesis of active pharmaceutical ingredients (APIs), medicinal chemistry, and chemical research
  • Not determined
  • 218.20 g/mol
  • Store in a tightly sealed container, in a cool, dry, and well-ventilated area away from light.
  • C8H5F3N2S
  • Not determined
  • 2 years when properly stored
  • Slightly soluble in water, soluble in organic solvents such as DMSO, methanol
  • Crystalline
  • 29349900
  • 126-130 C
  • 2-Amino-6-trifluoromethylbenzothiazole
  • Powder
  • Research chemical; Intermediate for pharmaceuticals, agrochemicals, and specialty chemicals
  • Off-white to pale yellow powder
  • 1.52 Gram per cubic centimeter(g/cm3)
  • >98%
  • Not classified as dangerous for transport
  • >110 C (estimated)
  • Stable under recommended storage conditions. Avoid moisture and strong oxidizers.
  • Warning
  • 2-8C recommended for long-term preservation
  • Not available; decomposes before boiling
  • Xn (Harmful) for precaution
  • Typically in 25 kg fiber drums or as required
  • For R&D or industrial use only; not for human or veterinary drug use

2-Amino-6- trifluoromethylbenzothiazole Trade Information

  • Mumbai
  • Cash in Advance (CID), Cash Advance (CA), Telegraphic Transfer (T/T)
  • 1000 Number Per Month
  • 7 Days
  • Yes
  • Sample costs shipping and taxes has to be paid by the buyer
  • North America, Africa, Asia, South America, Western Europe, Australia, Eastern Europe, Central America, Middle East
  • All India

Product Description

Chemical Name: 2-Amino-6-trifluoromethylbenzothiazole

Synonyms : 6-(trifluoromethyl)benzo[d]thiazol-2-amine|

6-(trifluoromethyl)-1,3-benzothiazol-2-amine|

2-amino-6-trifluoromethylbenzothiazole|

2-amino-6-(trifluoromethyl)-1,3-benzothiazole|

2-Amino-6-(trifluoromethyl)-1,3-benzothiazol|

6-Trifluoromethyl-benzothiazol-2-ylamine

CAS No : 777-12-8

Purity : 97%

MolecularFormula : C8H5F3N2S

Molecular Weight: 218.2

Appearance: Solid



Key Features and Benefits

This compound offers remarkable chemical stability and versatility for advanced synthesis. Suitable for both analytical and industrial grades, its high purity (>98%) ensures reliable performance in research and development. The electronegative trifluoromethyl group provides unique reactivity for diverse chemical processes, making it an essential component in the production of APIs and specialty products.


Safe Handling and Storage Recommendations

2-Amino-6-trifluoromethylbenzothiazole should be handled with care, as it may be harmful if swallowed. Always store the product in a cool, dry, and well-ventilated area, ideally at 2-8C. Ensure containers are tightly sealed and protected from moisture and strong oxidizing agents. Adhering to these guidelines helps maintain product integrity and ensures safe, long-term storage.


Applications in Chemical Research and Industry

Widely recognized as a valuable intermediate, this compound finds application in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactive properties with both electrophiles and nucleophiles allow for broad utility in medicinal chemistry, active pharmaceutical ingredient synthesis, and various research domains.

FAQ's of 2-Amino-6- trifluoromethylbenzothiazole:


Q: How should 2-Amino-6-trifluoromethylbenzothiazole be safely stored?

A: For optimal stability and preservation, store the compound in a tightly sealed container at 2-8C, in a cool, dry, and well-ventilated area, away from light, moisture, and strong oxidizing agents.

Q: What are the recommended applications for this compound?

A: 2-Amino-6-trifluoromethylbenzothiazole is used primarily as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It plays a key role in medicinal chemistry, active pharmaceutical ingredient production, and research development.

Q: When is it most beneficial to use this product?

A: This compound is most beneficial during research, chemical synthesis, or industrial processes that require a stable, reactive intermediate, particularly where the trifluoromethyl group can impart unique chemical or biological properties.

Q: Where can this product be transported or shipped?

A: As it is not classified as dangerous for transport, 2-Amino-6-trifluoromethylbenzothiazole can be shipped under standard conditions, typically in 25 kg fiber drums or customized packaging, in compliance with local regulations.

Q: What is the process for utilizing this compound in the lab?

A: To use 2-Amino-6-trifluoromethylbenzothiazole, dissolve it in a suitable organic solvent such as DMSO or methanol under the guidance of appropriate safety protocols. It can then be employed as a building block or intermediate in chemical reactions or synthesis procedures.

Q: What precautions should be taken during handling?

A: Handle with care as the substance may be harmful if ingested. Personal protective equipment, such as gloves, lab coat, and eye protection, is recommended. Use in a well-ventilated area and avoid skin or eye contact.

Q: How does the trifluoromethyl group enhance the compound's performance?

A: The presence of a trifluoromethyl group increases the compound's electronegativity and chemical stability, enabling unique reactivity with electrophiles and nucleophiles. This enhances its value as an intermediate in complex chemical syntheses.

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