7025-12-9 Usage
Tetrazole Ring System
1H-Tetrazole, 5-chloro-1-(4-chlorophenyl)contains a tetrazole ring system, which is a heterocyclic ring structure consisting of five members with four nitrogen atoms and one carbon atom.
Chlorophenyl Group
The compound also contains a chlorophenyl group, which is a phenyl ring (a six-membered carbon ring with alternating single and double bonds) with one or more chlorine atoms attached.
Heterocyclic Compound
1H-Tetrazole, 5-chloro-1-(4-chlorophenyl)is a heterocyclic compound, meaning it contains at least one ring structure with both carbon and non-carbon atoms.
Building Block in Organic Synthesis
1H-Tetrazole, 5-chloro-1-(4-chlorophenyl)- is often used as a building block in organic synthesis, meaning it can be used to create more complex organic molecules.
Potential Applications
1H-Tetrazole, 5-chloro-1-(4-chlorophenyl)has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and reactivity.
Stability
This chemical is considered to be stable under normal conditions, but it should be handled with care as it may pose hazards if not used properly.
Safety Protocols
It is important to follow proper safety protocols when working with 1H-Tetrazole, 5-chloro-1-(4-chlorophenyl)to ensure safe handling and use of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 7025-12-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7025-12:
(6*7)+(5*0)+(4*2)+(3*5)+(2*1)+(1*2)=69
69 % 10 = 9
So 7025-12-9 is a valid CAS Registry Number.
7025-12-9Relevant academic research and scientific papers
Synthesis of unsymmetrical sulfides derived from tetrazole-5-thiols
Hrabalek,Pus,Baranek,Kunes,Palat
, p. 183 - 189 (2007/10/03)
A series of unsymmetrical sulfides derived from I-substituted tetrazole-5-thiols was prepared by fusion of the corresponding 1-R-tetrazole-5-thiol sodium salt with 1-R′-5-halotetrazole. The structure was confirmed by 1H NMR and 13C NMR spectra. The target compounds were prepared in 50-80% yields.
