686747-49-9 Usage
Uses
Used in Chemical Production:
Benzothiazole, 2,5-dimethyl-6-nitro(9CI) is used as a precursor in the chemical industry for the production of dyes, pigments, and rubber chemicals. Its unique properties contribute to the development of these products, enhancing their performance and quality.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Benzothiazole, 2,5-dimethyl-6-nitro(9CI) is utilized as an intermediate in the synthesis of various organic compounds. Its chemical structure allows for the creation of new pharmaceuticals with potential therapeutic applications.
Used in Pesticide Production:
Benzothiazole, 2,5-dimethyl-6-nitro(9CI) may also be used in the production of pesticides, where its chemical properties can contribute to the effectiveness of these agricultural chemicals in controlling pests and diseases.
It is crucial to handle Benzothiazole, 2,5-dimethyl-6-nitro(9CI) with care due to its potential health hazards if not used properly, ensuring safety in its applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 686747-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,6,7,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 686747-49:
(8*6)+(7*8)+(6*6)+(5*7)+(4*4)+(3*7)+(2*4)+(1*9)=229
229 % 10 = 9
So 686747-49-9 is a valid CAS Registry Number.
686747-49-9Relevant articles and documents
STYRYLBENZOTHIAZOLE DERIVATIVES AND USES IN IMAGING
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Page/Page column 6; 53; 68-69, (2019/12/04)
This disclosure relates to styrylbenzothiazole derivatives for use as in vivo imaging agents for the diagnosis of Parkinson's disease (PD) or other degenerative disorders or conditions of the central nervous system. Early diagnosis is particularly advantageous as neuroprotective treatment can be applied to healthy neural cells to delay or even prevent the onset of debilitating clinical symptoms.
INHIBITORS OF 11-BETA-HYDROXY STEROID DEHYDROGENASE TYPE 1 AND TYPE 2
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Page/Page column 103, (2010/02/06)
There is provided a compound having Formula (I): wherein one of R1 and R2 is a group of the Formula (a), wherein R4 is selected from H and hydrocarbyl, R5 is a hydrocarbyl group and L is an optional linker group, or R1 and R2 together form a ring substituted with the group (Formula (a)) wherein R3 is H or a substituent, and wherein X is selected from S, O, NR6 and C(R7)(R8), wherein R6 is selected from H and hydrocarbyl groups, wherein each of R7 and R8 are independently selected from H and hydrocarbyl groups.