Cas 1450722-81-2,isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide

1450722-81-2

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Basic information

Product Name: isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide
Synonyms: isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide
CAS NO:1450722-81-2
Molecular Formula:
Molecular Weight: 330.411
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: isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide(1450722-81-2)
EPA Substance Registry System: isonicotinic acid N'-[1-amino-1-mercapto-3-(p-methoxyphenyl)-propen-1-yl]-hydrazide(1450722-81-2)

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: 1450722-81-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450722-81-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,7,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1450722-81:
(9*1)+(8*4)+(7*5)+(6*0)+(5*7)+(4*2)+(3*2)+(2*8)+(1*1)=142
142 % 10 = 2
So 1450722-81-2 is a valid CAS Registry Number.

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1450722-81-2Relevant academic research and scientific papers

Synthesis and bioevaluation of some new isoniazid derivatives

Matei, Lilia,Bleotu, Coralia,Baciu, Ion,Draghici, Constantin,Ionita, Petre,Paun, Anca,Chifiriuc, Mariana Carmen,Sbarcea, Adriana,Zarafu, Irina

, p. 5355 - 5361 (2013/09/02)

The aim of the study was to synthesize some new compounds with potential anti-tuberculosis activity, containing isoniazid and α,β-unsaturated thiocinnamamide-like thioamides as precursors. The obtained derivatives were evaluated regarding their biological

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