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7-Azabicyclo[4.2.2]decan-8-one, 5-ethenylidene-7-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88996-17-2

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88996-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88996-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,9 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88996-17:
(7*8)+(6*8)+(5*9)+(4*9)+(3*6)+(2*1)+(1*7)=212
212 % 10 = 2
So 88996-17-2 is a valid CAS Registry Number.

88996-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-benzyl-5-ethenylidene-7-azabicyclo[4.2.2]decan-8-one

1.2 Other means of identification

Product number -
Other names 7-Azabicyclo[4.2.2]decan-8-one,5-ethenylidene-7-(phenylmethyl)

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:88996-17-2 SDS

88996-17-2Downstream Products

88996-17-2Relevant academic research and scientific papers

INTRAMOLECULAR REACTIONS OF-PROPYNYLSILANES WITH N-ACYLIMINIUM; CUPRATES SN2' REACTIONS OF THE ALLENIC PRODUCTS AS A ROUTE TO TRANS-FUSED CARBOBICYCLES

Klaver, Wim J.,Moolenaar, Marinus J.,Hiemstra, Henk,Speckamp, W. Nico

, p. 3805 - 3818 (2007/10/02)

Intramolecular acid-assisted reactions of 2-propynylsilanes with cyclic N-acyliminium ion precursors lead to bridged azabicyclic systems 34-45 (Table I), containing the uncommon α-allenic amide funcionality.After introduction of a tert-butoxycarbonyl or a

ω-Alkoxy Lactams as Dipolar Synthons. Silicon-Assisted Synthesis of Azabicycles and a γ-Amino Acid

Hiemstra, Henk,Klaver, Wim J.,Speckamp, W. Nico

, p. 1149 - 1151 (2007/10/02)

Alkylation of the lithium enolates derived from ω-alkoxy lactams 1a-c with unsaturated iodides 4 affords 5 in high yields (Table I).Those alkylation products 5, which contain an allyl- or propargylsilane moiety, undergo cyclization on acid treatment to fu

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