Cas 1279116-31-2,7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one

1279116-31-2

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Basic information

Product Name: 7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one
Synonyms: 7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one
CAS NO:1279116-31-2
Molecular Formula:
Molecular Weight: 405.324
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: 7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one(1279116-31-2)
EPA Substance Registry System: 7-chloro-4-((4-(2-chlorophenyl)piperazin-1-yl)methyl)-3,4-dihydro-benzo[b]oxepin-5(2H)-one(1279116-31-2)

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: 1279116-31-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1279116-31-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,1,1 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1279116-31:
(9*1)+(8*2)+(7*7)+(6*9)+(5*1)+(4*1)+(3*6)+(2*3)+(1*1)=162
162 % 10 = 2
So 1279116-31-2 is a valid CAS Registry Number.

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1279116-31-2Relevant academic research and scientific papers

Benzoxepin derivatives: Design, synthesis, and pharmacological evaluation with sedative-hypnotic effect

Abdel Gawad, Nagwa M.,Hassan, Ghaneya S.,Georgey, Hanan H.,El-Zorba, Hesham Y.

, p. 747 - 759 (2012)

A series of novel benzoxepin-derived compounds were synthesized and evaluated for their sedative- hypnotic effect using Phenobarbital-induced sleep test in mice. Compound 6 in which the Phenobarbital moiety was incorporated into the benzoxepin nucleus was

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