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2-Amino-6- trifluoromethylbenzothiazole

2-Amino-6- trifluoromethylbenzothiazole

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Product Details:

  • Molecular Formula C8H5F3N2S
  • CAS No 777-12-8
  • Product Type Pharmaceutical Intermediate; Organic Chemical
  • Density 1.52 Gram per cubic centimeter(g/cm3)
  • Smell Characteristic benzothiazole-like odor
  • Usage Used in synthesis of active pharmaceutical ingredients (APIs), medicinal chemistry, and chemical research
  • Properties High chemical stability; Electronegative trifluoromethyl group; Reacts with electrophiles and nucleophiles
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2-Amino-6- trifluoromethylbenzothiazole Price And Quantity

  • 1 Number

2-Amino-6- trifluoromethylbenzothiazole Product Specifications

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

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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