Cas 97064-77-2,3-(4-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride

97064-77-2

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Basic information

Product Name: 3-(4-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride
Synonyms: 3-(4-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride
CAS NO:97064-77-2
Molecular Formula:
Molecular Weight: 398.356
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-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride(97064-77-2)
EPA Substance Registry System: 3-(4-Azepan-1-yl-but-2-ynyl)-5-(4-chloro-phenyl)-3H-[1,3,4]thiadiazol-2-one; hydrochloride(97064-77-2)

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: 97064-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97064-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,6 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97064-77:
(7*9)+(6*7)+(5*0)+(4*6)+(3*4)+(2*7)+(1*7)=162
162 % 10 = 2
So 97064-77-2 is a valid CAS Registry Number.

97064-77-2Upstream product

97064-77-2Downstream Products

97064-77-2Relevant 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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