Cas 1206190-36-4,3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide

1206190-36-4

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Basic information

Product Name: 3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide
Synonyms: 3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide
CAS NO:1206190-36-4
Molecular Formula:
Molecular Weight: 354.409
EINECS: N/A
Product Categories: N/A
Mol File: 1206190-36-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide(1206190-36-4)
EPA Substance Registry System: 3-phenyl-5-(3,4,5-trimethoxyphenyl)-4,5-dihydro-1H-pyrazole-1-carboximidamide(1206190-36-4)

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: 1206190-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1206190-36-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,1,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1206190-36:
(9*1)+(8*2)+(7*0)+(6*6)+(5*1)+(4*9)+(3*0)+(2*3)+(1*6)=114
114 % 10 = 4
So 1206190-36-4 is a valid CAS Registry Number.

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1206190-36-4Relevant articles and documents

Efficient sonochemical synthesis of novel 3,5-diaryl-4,5-dihydro-1H-pyrazole-1-carboximidamides

Pizzuti, Lucas,Martins, Paula L.G.,Ribeiro, Bruna A.,Quina, Frank H.,Pinto, Ernani,Flores, Alex F.C.,Venzke, Dalila,Pereira, Claudio M.P.

experimental part, p. 34 - 37 (2010/11/16)

An ultrasound-assisted preparation of a series of novel 3,5-diaryl-4,5-dihydro-1H-pyrazole-1-carboximidamides that proceeds via the efficient reaction of chalcones with aminoguanidine hydrochloride under clean conditions is described.

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