Cas 172845-73-7,5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester

172845-73-7

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Basic information

Product Name: 5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester
Synonyms: 5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester
CAS NO:172845-73-7
Molecular Formula:
Molecular Weight: 465.36
EINECS: N/A
Product Categories: N/A
Mol File: 172845-73-7.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: 5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(172845-73-7)
EPA Substance Registry System: 5-Amino-3-benzylsulfanyl-1-(3,4-dichloro-phenylcarbamoyl)-1H-pyrazole-4-carboxylic acid ethyl ester(172845-73-7)

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: 172845-73-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172845-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,8,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172845-73:
(8*1)+(7*7)+(6*2)+(5*8)+(4*4)+(3*5)+(2*7)+(1*3)=157
157 % 10 = 7
So 172845-73-7 is a valid CAS Registry Number.

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172845-73-7Relevant articles and documents

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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