Cas 204445-25-0,methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide

204445-25-0

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Basic information

Product Name: methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide
Synonyms: methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide
CAS NO:204445-25-0
Molecular Formula: C20H24N2S
Molecular Weight: 324.48296
EINECS: N/A
Product Categories: N/A
Mol File: 204445-25-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide(204445-25-0)
EPA Substance Registry System: methyl 2-(3-phenyl-1H-pyrazol-1-yl)-2-adamantyl sulfide(204445-25-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 204445-25-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 204445-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,4,4 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 204445-25:
(8*2)+(7*0)+(6*4)+(5*4)+(4*4)+(3*5)+(2*2)+(1*5)=100
100 % 10 = 0
So 204445-25-0 is a valid CAS Registry Number.

204445-25-0Upstream product

2458-26-6 3-phenylpyrazole

204445-25-0Downstream Products

204445-25-0Relevant academic research and scientific papers

Trapping of thiocarbonyl ylides with NH-azoles; A novel route to N-substituted azoles

Mloston,Gendek,Heimgartner

, p. 66 - 72 (2007/10/03)

Thermal decomposition of 2,5-dihydro-1,3,4-thiadiazoles (1) in the presence of imidazole, pyrazole, 3-phenylpyrazole, and 1,2,4-triazole, respectively, yielded S,N-acetals of type 4. Interception of initially formed thiocarbonyl ylide 2 by the NH-azole is proposed as the reaction mechanism. Treatment of the S,N-acetals 4 with Raney-Ni gave N-substituted azoles 6.

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