6361-41-7 Usage
Description
2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) is an organic compound with the molecular formula C10H9NO4S. It is a derivative of naphthalene, featuring an acetamido group, a hydroxyl group, and a sulfonic acid group. 2-Acetamido-8-naphthol-6-sufonic acid (N-acetyl gamma acid) is known for its versatile chemical properties and potential applications in various industries.
Uses
Used in Chemical Synthesis:
2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) is used as an intermediate in the chemical synthesis of various compounds, particularly in the preparation of anthraquinone dyes. Its unique structure allows for further functionalization and modification, making it a valuable building block in the synthesis of complex organic molecules.
Used in Microbial Studies:
In the field of microbiology, 2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) is utilized for the preparation of anthraquinone dyes, which are essential for various microbial studies. These dyes are used to stain and visualize microorganisms, aiding in the identification and classification of different species.
Used in Pharmaceutical Industry:
2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) may also find applications in the pharmaceutical industry, potentially serving as a precursor for the development of new drugs or as a component in drug formulations. Its chemical properties and reactivity make it a promising candidate for further research and development in this field.
Used in Dye Manufacturing:
In the dye manufacturing industry, 2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) is used in the production of anthraquinone dyes. These dyes are widely used in various applications, including textiles, plastics, and printing inks, due to their vibrant colors and stability.
Used in Research and Development:
Due to its unique chemical structure and properties, 2-Acetamido-8-naphthol-6-sulfonic acid (N-acetyl gamma acid) is also used in research and development for exploring new applications and understanding its potential interactions with other compounds. This can lead to the discovery of new uses and advancements in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 6361-41-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6361-41:
(6*6)+(5*3)+(4*6)+(3*1)+(2*4)+(1*1)=87
87 % 10 = 7
So 6361-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO5S/c1-7(14)13-9-3-2-8-4-10(19(16,17)18)6-12(15)11(8)5-9/h2-6,15H,1H3,(H,13,14)(H,16,17,18)
6361-41-7Relevant articles and documents
Triazinyl reactive dyes containing additional fiber reactive groups bound through the sulfonylalkylaminoalkylamino bridge
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, (2008/06/13)
The invention relates to novel useful reactive dyes of the formula I STR1 in which: F is a radical selected from the group consisting of metal-free or metal-containing monoazo or disazo dyes containing at least one --SO3 H group, anthraquinone dyes, sulfophthalocyanine dyes, formazan dyes, phenazine dyes, oxanine dyes and nitroaryl dyes, R is hydrogen, C1 -C4 alkyl which is unsubstituted or substituted with --COOH or --SO3 H, cyanoethyl, or hydroxyethyl, X is fluorine, chlorine, bromine, --SO3 H, phenylsulfonyl or C1 -C4 -alkylsulfonyl, P is 1 or 2 and A is a radical of the formula STR2 in which: the groups designated "alk" are independently of each other straight or branched polymethylene radicals having 2 to 6 carbon atoms, and Z is β-halogenoethyl, vinyl, β-sulfatoethyl, β-thiosulfatoethyl or βacetoxyethyl.
