Cas 144836-10-2,[2-(4-Chloro-phenyl)-4-oxo-4H-pyrazolo[1,5-d][1,2,4]triazin-5-yl]-acetic acid

144836-10-2

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Basic information

Product Name: [2-(4-Chloro-phenyl)-4-oxo-4H-pyrazolo[1,5-d][1,2,4]triazin-5-yl]-acetic acid
Synonyms:
CAS NO:144836-10-2
Molecular Formula:
Molecular Weight: 304.692
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: [2-(4-Chloro-phenyl)-4-oxo-4H-pyrazolo[1,5-d][1,2,4]triazin-5-yl]-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: [2-(4-Chloro-phenyl)-4-oxo-4H-pyrazolo[1,5-d][1,2,4]triazin-5-yl]-acetic acid(144836-10-2)
EPA Substance Registry System: [2-(4-Chloro-phenyl)-4-oxo-4H-pyrazolo[1,5-d][1,2,4]triazin-5-yl]-acetic acid(144836-10-2)

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: 144836-10-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144836-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,8,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144836-10:
(8*1)+(7*4)+(6*4)+(5*8)+(4*3)+(3*6)+(2*1)+(1*0)=132
132 % 10 = 2
So 144836-10-2 is a valid CAS Registry Number.

144836-10-2Upstream product

135104-22-2 2-(4-Chloro-phenyl)-5H-pyrazolo[1,5-d][1,2,4]triazin-4-one

144836-10-2Downstream Products

144836-10-2Relevant academic research and scientific papers

Synthesis and aldose reductase inhibitory activity of triazine derivatives possessing acetic acid group

Mavel,Coudert,Albuisson,Duroux,Bastide,Couquelet,Tronche,Rubat

, p. 1411 - 1414 (2007/10/02)

N-Acetic acid derivatives of 6-aryl-pyrazolo-triazin-4-ones were synthesized for evaluation as new aldose reductase inhibitors. The intrinsic activity of each compound was assessed by measuring the inhibition of enzymatic activity in an isolated pig lens

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