Cas 180726-96-9,5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester

180726-96-9

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Basic information

Product Name: 5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester
Synonyms: 5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester
CAS NO:180726-96-9
Molecular Formula:
Molecular Weight: 430.915
EINECS: N/A
Product Categories: N/A

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: 5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(180726-96-9)
EPA Substance Registry System: 5-Amino-3-benzylsulfanyl-1-(4-chloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(180726-96-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 180726-96-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 180726-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,7,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 180726-96:
(8*1)+(7*8)+(6*0)+(5*7)+(4*2)+(3*6)+(2*9)+(1*6)=149
149 % 10 = 9
So 180726-96-9 is a valid CAS Registry Number.

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180726-96-9Relevant academic research and scientific papers

Synthesis of 3-(1-arylaminocarbonyl-5-amino)-1,2,4-triazolyl benzyl sulfide, sulfoxide and sulfone

Lu, Rongjian,Yang, Huazheng,Zhao, Guofeng,Liu, Huayin,Shang, Zhenfeng

, p. 221 - 230 (2007/10/03)

3-(1-arylaminocarbonyl-5-amino)-1,2,4-triazolyl benzyl sulfides were synthesized by the reaction of 5-amino-3-benzylthio-1,2,4-triazole and its analogue with the aryl isocyanate. It was found that there was great influence by the property and position of

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