120740-09-2 Usage
Heterocyclic compound
It contains a chlorothiazole group and an isoindole-1,3-dione group The compound is made up of multiple rings with different elements, making it a complex structure with various functional groups.
Chlorothiazole group
2-chloro-1,3-thiazol-5-yl A five-membered ring structure with one sulfur atom, three nitrogen atoms, and one chlorine atom attached to the 2-position.
Isoindole-1,3-dione group
1H-isoindole-1,3(2H)-dione A bicyclic structure with a fused benzene ring and a five-membered ring, containing two carbonyl groups (C=O) at the 1 and 3 positions.
Potential pharmaceutical properties
It may be used in medicinal chemistry research 2-[(2-CHLORO-1,3-THIAZOL-5-YL)METHYL]-1H-ISOINDOLE-1,3(2H)-DIONE has the potential to be developed into a drug or serve as a building block for other pharmaceuticals due to its unique structure and properties.
Safety precautions
Handle with care and follow proper safety protocols Due to possible toxic or harmful effects, it is essential to take necessary precautions while working with this chemical to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 120740-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,7,4 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120740-09:
(8*1)+(7*2)+(6*0)+(5*7)+(4*4)+(3*0)+(2*0)+(1*9)=82
82 % 10 = 2
So 120740-09-2 is a valid CAS Registry Number.
120740-09-2Relevant academic research and scientific papers
Process for the preparation of chlorothiazole derivatives
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, (2008/06/13)
Novel processes for preparing 2-chlorothiazoles, useful as an intermediate for insecticides, from allyl isothiocyanate derivatives having the formula [II]: STR1 wherein X represents a leaving group, are simple and convenient reaction procedures under mild conditions without need of a large excess of a chlorinating agent. Further, processes for preparing 5-(aminomethyl)-2-chlorothiazole or salts thereof from the compound [II] achieve higher yields by simple, convenient and inexpensive procedures.
