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α,α-bis(pyrazol-1-yl)toluene is an organic compound characterized by its unique structure, which consists of a toluene core with two pyrazole rings attached to the alpha carbon atoms. Pyrazole is a five-membered heterocyclic ring containing three nitrogen atoms, which imparts specific electronic and steric properties to the molecule. α,α-bis(pyrazol-1-yl)toluene is of interest in various fields, including coordination chemistry, where it can act as a bidentate ligand due to the presence of two pyrazole rings. It is also used in the synthesis of more complex organic molecules and materials, such as pharmaceuticals and dyes. The compound's stability, reactivity, and potential applications make it a subject of study in chemical research and development.

40848-73-5

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Basic information
1. Product Name: α,α-bis(pyrazol-1-yl)toluene
2. Synonyms: α,α-bis(pyrazol-1-yl)toluene
3. CAS NO:40848-73-5
4. Molecular Formula:
5. Molecular Weight: 224.265
6. EINECS: N/A
7. Product Categories: N/A
Chemical Properties
1. Melting Point: N/A
2. Boiling Point: N/A
3. Flash Point: N/A
4. Appearance: N/A
5. Density: N/A
6. Refractive Index: N/A
7. Storage Temp.: N/A
8. Solubility: N/A
9. CAS DataBase Reference: α,α-bis(pyrazol-1-yl)toluene(CAS DataBase Reference)
10. NIST Chemistry Reference: α,α-bis(pyrazol-1-yl)toluene(40848-73-5)
11. EPA Substance Registry System: α,α-bis(pyrazol-1-yl)toluene(40848-73-5)
Safety Data
1. Hazard Codes: N/A
2. Statements: N/A
3. Safety Statements: N/A
4. WGK Germany:
5. RTECS:
6. HazardClass: N/A
7. PackingGroup: N/A
8. Hazardous Substances Data: 40848-73-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 40848-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,4 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40848-73:
(7*4)+(6*0)+(5*8)+(4*4)+(3*8)+(2*7)+(1*3)=125
125 % 10 = 5
So 40848-73-5 is a valid CAS Registry Number.

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40848-73-5Relevant academic research and scientific papers

REACTIVITY OF AZOLES TOWARDS BENZALDEHYDE AND ITS DIMETHYLACETAL. SYNTHESIS OF N,N'-DIAZOLYLPHENYLMETHANES

Ballesteros, P.,Elguero, J.,Claramunt, R. M.

, p. 5955 - 5964 (2007/10/02)

Some 1,1'-diindazolylphenylmethanes have been prepared from indazoles and benzaldehyde in presence of zinc chloride as catalyst.The reaction was strongly dependent on the basic pKa's of azoles and only few pyrazolyl derivatives could be prepare

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