Cas 97051-10-0,3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride

97051-10-0

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Basic information

Product Name: 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride
Synonyms: 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride
CAS NO:97051-10-0
Molecular Formula:
Molecular Weight: 401.36
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: 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride(97051-10-0)
EPA Substance Registry System: 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride(97051-10-0)

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: 97051-10-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97051-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,5 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97051-10:
(7*9)+(6*7)+(5*0)+(4*5)+(3*1)+(2*1)+(1*0)=130
130 % 10 = 0
So 97051-10-0 is a valid CAS Registry Number.

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97051-10-0Relevant academic research and scientific papers

Synthesis and biological evaluation of 5-aryl-3-(4-tert-amino-2-butynyl)-1,3,4-thiadiazol-2 (3H)-ones

Muhi-Eldeen,Eldine,Al-Jawad,et al.

, p. 33 - 36 (2007/10/02)

A series of 5-aryl-3-(4-tert-amino-2-butynyl)-1,3,4-thiadiazol-2 (3H)-ones has been prepared and investigated for blocking motor effects of oxotremorine in intact mice and for their antagonistic activity towards acetylcholine on isolated guinea pig ileal

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