Basic information

Product Name: Piperidine, 1-[2-(2-nitrophenyl)ethenyl]-, (E)-
Synonyms:
CAS NO:61293-28-5
Molecular Formula: C13H16N2O2
Molecular Weight: 232.282
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: Piperidine, 1-[2-(2-nitrophenyl)ethenyl]-, (E)-(CAS DataBase Reference)
NIST Chemistry Reference: Piperidine, 1-[2-(2-nitrophenyl)ethenyl]-, (E)-(61293-28-5)
EPA Substance Registry System: Piperidine, 1-[2-(2-nitrophenyl)ethenyl]-, (E)-(61293-28-5)

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: 61293-28-5(Hazardous Substances Data)

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61293-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61293-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,9 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61293-28:
(7*6)+(6*1)+(5*2)+(4*9)+(3*3)+(2*2)+(1*8)=115
115 % 10 = 5
So 61293-28-5 is a valid CAS Registry Number.

61293-28-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	trans-2-nitro-β-piperidinostyrene

1.2 Other means of identification

Product number	-
Other names	1-[(E)-2-(2-Nitro-phenyl)-vinyl]-piperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:61293-28-5 SDS

61293-28-5Upstream product

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61293-28-5Relevant academic research and scientific papers

Intermediates for indoles

-

, (2008/06/13)

Ortho-nitrotoluenes are condensed with formamide acetals to yield the corresponding otho-nitro-β-aminestyrenes which undergo cyclization upon reduction to yield indoles.

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