76002-68-1 Usage
Uses
Used in Pharmaceutical Industry:
6,7-Dichloro-quinoxalin-2-ylamine serves as a crucial building block in the synthesis of various drug molecules, playing a significant role in the development of new pharmaceuticals. Its unique chemical structure allows for the creation of compounds with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agricultural Chemicals:
Beyond its pharmaceutical applications, 6,7-Dichloro-quinoxalin-2-ylamine may also find use in the agricultural sector. Its potential role in the development of agricultural chemicals could include the creation of pesticides or other compounds designed to enhance crop protection and yield.
Used as a Dye Intermediate:
In the realm of dye manufacturing, 6,7-Dichloro-quinoxalin-2-ylamine holds promise as an intermediate. Its chemical properties make it suitable for use in the synthesis of dyes with specific color characteristics, thereby expanding the range of dyes available for various industrial applications.
Safety Considerations:
Given the potentially hazardous nature of 6,7-Dichloro-quinoxalin-2-ylamine, it is essential that this compound is handled with care. Adherence to proper safety guidelines is mandatory to mitigate risks associated with its use, ensuring the safety of both individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 76002-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76002-68:
(7*7)+(6*6)+(5*0)+(4*0)+(3*2)+(2*6)+(1*8)=111
111 % 10 = 1
So 76002-68-1 is a valid CAS Registry Number.
76002-68-1Relevant articles and documents
Synthesis and oral antiallergic activity of carboxylic acids derived from imidazo[2,1-c][1,4]benzoxazines, imidazo[1,2-a]quinolines, imidazo[1,2-a]quinoxalines, imidazo[1,2-a]quinoxalinones, pyrrolo[1,2-a]quinoxalinones, pyrrolo[2,3-a]quinoxalinones, and
Ager,Barnes,Danswan,Hairsine,Kay,Kennewell,Matharu,Miller,Robson,Rowlands,Tully,Westwood
, p. 1098 - 1115 (2007/10/02)
4H-Imidazo[2,1-c][1,4]benzoxazine-1-carboxylic acid (3) was found to possess potent activity in the IgE-induced rat passive cutaneous anaphylaxis model which may be predictive of clinical antiallergic activity. Compared to disodium cromoglycate (DSCG,1),
Novel imidazoquinoxalines
-
, (2008/06/13)
Novel imidazoquinoxalines of the formula STR1 wherein R is selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms, --NH4, alkali metal, alkaline earth metal, magnesium, aluminum and non-toxic, pharmaceutically acceptable amines, X is selected from the group consisting of hydrogen, alkoxy of 1 to 5 carbon atoms and carbamoyl and Y and Z are individually selected from the group consisting of hydrogen and halogen and their non-toxic, pharmaceutically acceptable acid addition salts having anti-allergic activity and their preparation.
