Cas 61326-06-5,4-[4-(4-chlorobenzyl)piperazin-1-yl]-2-ethyl-7-fluoro-5H-thieno[2,3-b][1,5]benzodiazepine

61326-06-5

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Basic information

Product Name: 4-[4-(4-chlorobenzyl)piperazin-1-yl]-2-ethyl-7-fluoro-5H-thieno[2,3-b][1,5]benzodiazepine
Synonyms:
CAS NO:61326-06-5
Molecular Formula: C₂₄H₂₄ClFN₄S
Molecular Weight: 454.9906
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 572.6°C at 760 mmHg
Flash Point: 300.1°C
Appearance: N/A
Density: 1.36g/cm³
Vapor Pressure: 4.03E-13mmHg at 25°C
Refractive Index: 1.684
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-[4-(4-chlorobenzyl)piperazin-1-yl]-2-ethyl-7-fluoro-5H-thieno[2,3-b][1,5]benzodiazepine(CAS DataBase Reference)
NIST Chemistry Reference: 4-[4-(4-chlorobenzyl)piperazin-1-yl]-2-ethyl-7-fluoro-5H-thieno[2,3-b][1,5]benzodiazepine(61326-06-5)
EPA Substance Registry System: 4-[4-(4-chlorobenzyl)piperazin-1-yl]-2-ethyl-7-fluoro-5H-thieno[2,3-b][1,5]benzodiazepine(61326-06-5)

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: 61326-06-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 61326-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61326-06:
(7*6)+(6*1)+(5*3)+(4*2)+(3*6)+(2*0)+(1*6)=95
95 % 10 = 5
So 61326-06-5 is a valid CAS Registry Number.

61326-06-5Upstream product

61326-06-5Downstream Products

61326-06-5Relevant academic research and scientific papers

4-Piperazinyl-10H-thienobenzodiazepines as Potential Neuroleptics

Chakrabarti, Jiban K.,Horsman, Linda,Hotten, Terrence M.,Pullar, Ian A.,Tupper, David E.

, p. 878 - 884 (2007/10/02)

A series of 4-substituted 10H-thienobenzodiazepines has been synthesized.These compounds have been assessed for their ability to block a conditioned avoidance response (CAR) and to produce catalepsy in rats and have been compared with several

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