128104-82-5 Usage
Uses
Used in Dye and Pigment Production:
(1-Chloro-3,4-dihydro-2-naphthalenyl)methanol is used as a reactive dye intermediate for the production of various dyes and pigments, contributing to the coloration of different materials.
Used in Textile Industry:
In the textile industry, (1-Chloro-3,4-dihydro-2-naphthalenyl)methanol is used as a colorant to impart specific shades and hues to fabrics, enhancing their visual appeal and durability.
Used in Paper Industry:
(1-Chloro-3,4-dihydro-2-naphthalenyl)methanol is utilized as a colorant in the paper industry to improve the appearance and quality of paper products.
Used in Pharmaceutical Synthesis:
This chemical is employed in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medicinal compounds.
Used as a Research Chemical:
(1-Chloro-3,4-dihydro-2-naphthalenyl)methanol is used as a research chemical in laboratories, aiding scientists in conducting experiments and advancing chemical research.
Safety Precautions:
It is important to handle (1-Chloro-3,4-dihydro-2-naphthalenyl)methanol with caution, as it may be harmful if inhaled, ingested, or comes into contact with the skin. Proper safety precautions and protective equipment should be used when working with this chemical to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 128104-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128104-82:
(8*1)+(7*2)+(6*8)+(5*1)+(4*0)+(3*4)+(2*8)+(1*2)=105
105 % 10 = 5
So 128104-82-5 is a valid CAS Registry Number.
128104-82-5Relevant articles and documents
Antihyperglycemic activity of novel substituted 3H-1,2,3,5-oxathiadiazole 2-oxides
Ellingboe,Alessi,Dolak,Nguyen,Tomer,Guzzo,Bagli,McCaleb
, p. 1176 - 1183 (2007/10/02)
A series of substituted 3H-1,2,3,5-oxathiadiazole-2-oxides (6) was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus. The oxathiadiazoles 6 were synthesized by a two-step sequence: treatment of a substituted acetonitrile (4) with hydroxylamine to give the corresponding amidoxime (5) and cyclization with thionyl chloride to yield 6. In terms of potency, the 2-naphthalenylmethyl group (as in compound 3) was found to be the optimal substituent in this series. Compound 3 was approximately 5 times more potent than ciglitazone (1).
Novel substituted 3H-1,2,3,5-oxathiadiazole 2-oxides useful as anthihyperglycemic agents
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, (2008/06/13)
This invention relates to novel substituted 3H-1,2,3,5-oxathiadiazole 2-oxides, to the processes for their preparation, to methods for using the compounds, and to pharmaceutical compositions thereof. The compounds have pharmaceutical properties which render them beneficial for the treatment of diabetes mellitus and associated conditions.
