Cas 1609483-24-0,ethyl 1-(4-(4-chlorophenyl)-5-methylthiazol-2-yl)-5-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate

1609483-24-0

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Basic information

Product Name: ethyl 1-(4-(4-chlorophenyl)-5-methylthiazol-2-yl)-5-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate
Synonyms:
CAS NO:1609483-24-0
Molecular Formula:
Molecular Weight: 506.84
EINECS: N/A
Product Categories: N/A
Mol File: 1609483-24-0.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: ethyl 1-(4-(4-chlorophenyl)-5-methylthiazol-2-yl)-5-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-(4-(4-chlorophenyl)-5-methylthiazol-2-yl)-5-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate(1609483-24-0)
EPA Substance Registry System: ethyl 1-(4-(4-chlorophenyl)-5-methylthiazol-2-yl)-5-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylate(1609483-24-0)

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: 1609483-24-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609483-24-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1609483-24:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*8)+(3*3)+(2*2)+(1*4)=180
180 % 10 = 0
So 1609483-24-0 is a valid CAS Registry Number.

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1609483-24-0Relevant articles and documents

An efficient one-pot synthesis of aryl-substituted 1-(thiazol-2-yl)-1H- pyrazole-3-carboxylates via a hantzsch synthesis-knorr reaction sequence

Gu, Chunhui,Zhai, Jiaojiao,Jiang, Jianan,Liu, Hongwei,Wang, Lei,Zhu, Dunru,Ji, Yafei

supporting information, p. 179 - 190 (2014/03/21)

The treatment of α-bromoalkyl aryl ketones and 2-(propan-2-ylidene) hydrazine carbothioamide afforded 4-aryl-2-(2-(propan-2-ylidene)hydrazinyl) thiazoles via a Hantzsch-thiazole synthesis, which reacted with 4-aryl-2,4-diketoesters via a sequential Knorr-

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