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1-[(E)-pent-2-en-3-yl]piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21086-43-1

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21086-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21086-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,8 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21086-43:
(7*2)+(6*1)+(5*0)+(4*8)+(3*6)+(2*4)+(1*3)=81
81 % 10 = 1
So 21086-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H19N/c1-3-10(4-2)11-8-6-5-7-9-11/h3H,4-9H2,1-2H3/b10-3+

21086-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-pent-2-en-3-ylpiperidine

1.2 Other means of identification

Product number -
Other names 3-Piperidino-penten-2

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:21086-43-1 SDS

21086-43-1Relevant academic research and scientific papers

THE REACTION OF TRICHLOROSILANE WITH ENAMINES

Snyder, Dudley C.

, p. 137 - 144 (2007/10/02)

A previously unknown reaction of trichlorosilane with enamines has been discovered and a preliminary study done on the possible mechanism.The products of the reaction are a regiospecific trichlorosilyl adduct resulting from addition of the trichlorosilane to the enamine unsaturation and the amine corresponding to simple reduction of the double bond.The addition of the trichlorosilane requires no catalyst and the relative percentages of the products varies in a generally inverse fashion depending on the exact structure of the enamine.Evidence is given to support the assigned structure of the trichlorosilyl species and mechanisms are hypothesized to explain the formation of both products from a common intermediate.Steric rather than electronic factors are suggested as responsible for the observed balance between them.

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