172681-47-9 Usage
Uses
Used in Research and Development:
2-AMINO-6-IODOTOLUENE is used as a research reagent for organic synthesis and other chemical processes. Its unique structure and reactivity make it a valuable tool for chemists and researchers working on the development of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-AMINO-6-IODOTOLUENE is used as an intermediate in the synthesis of various drugs and pharmaceutical compounds. Its ability to react with other molecules and form new chemical entities makes it a versatile building block in the development of novel therapeutic agents.
Used in Chemical Synthesis:
2-AMINO-6-IODOTOLUENE is also used as a key component in the synthesis of various organic compounds, including dyes, pigments, and other specialty chemicals. Its unique properties allow it to be easily incorporated into complex molecular structures, contributing to the development of new products with specific applications and functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 172681-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,6,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 172681-47:
(8*1)+(7*7)+(6*2)+(5*6)+(4*8)+(3*1)+(2*4)+(1*7)=149
149 % 10 = 9
So 172681-47-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8IN/c1-5-6(8)3-2-4-7(5)9/h2-4H,9H2,1H3
172681-47-9Relevant articles and documents
4-Substituted indazoles as new inhibitors of neuronal nitric oxide synthase
Boulouard, Michel,Schumann-Bard, Pascale,Butt-Gueulle, Sabrina,Lohou, Elodie,Stiebing, Silvia,Collot, Valerie,Rault, Sylvain
, p. 3177 - 3180 (2008/02/04)
A series of halo-1-H-indazoles has been synthesized and evaluated for its inhibitory activity on neuronal nitric oxide synthase. Introduction of bromine at the C4 position of the indazole ring system provided a compound almost as potent as the reference compound, that is, 7-nitroindazole (7-NI). The importance of position 4 is further demonstrated by the synthesis and pharmacological evaluation of the 4-nitroindazole which was also a potent inhibitor of NOS activity. These compounds also exhibited in vivo NOS inhibitory activity, as attested by potent antinociceptive effects following systemic administration.
4- and 5-Substituted 2,3-dihydro-1H-isoindoles, pharmaceutical compositions and method of inhibiting phenylethanolamine N-methyltransferase
-
, (2008/06/13)
Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase using novel 2,3-dihydro-1H-isoindole compounds having 4- and 5-substituents.
