Cas 1092847-77-2,tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate

1092847-77-2

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Basic information

Product Name: tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate
Synonyms: tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate
CAS NO:1092847-77-2
Molecular Formula:
Molecular Weight: 337.806
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: tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate(1092847-77-2)
EPA Substance Registry System: tert-butyl 4-(5-chlorobenzo[d]oxazol-2-yl)piperazine-1-carboxylate(1092847-77-2)

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: 1092847-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092847-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,8,4 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1092847-77:
(9*1)+(8*0)+(7*9)+(6*2)+(5*8)+(4*4)+(3*7)+(2*7)+(1*7)=182
182 % 10 = 2
So 1092847-77-2 is a valid CAS Registry Number.

1092847-77-2Upstream product

1092847-77-2Downstream Products

140233-44-9 5-chloro-2-(piperazin-1-yl)benzooxazole

1092847-77-2Relevant academic research and scientific papers

TRIAZOLE DERIVATIVES HAVING ANTIFUNGAL ACTIVITY, METHOD FOR THE PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 29, (2009/01/24)

A triazole derivative of formula 1 or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof is superior to the conventional antifungal drugs in antifungal activity against a wide spectrum of pathogenic fungi, and has advantageously low toxicity.

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