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N,N-diethyl-2-(1H-inden-3-yl)ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14585-67-2

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14585-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14585-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,8 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14585-67:
(7*1)+(6*4)+(5*5)+(4*8)+(3*5)+(2*6)+(1*7)=122
122 % 10 = 2
So 14585-67-2 is a valid CAS Registry Number.

14585-67-2SDS

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 N,N-diethyl-2-(3H-inden-1-yl)ethanamine

1.2 Other means of identification

Product number -
Other names Indene-3-ethylamine,N,N-diethyl

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:14585-67-2 SDS

14585-67-2Relevant academic research and scientific papers

Chiral silicon-bridged 2-(N,N-dialkylamino)ethyl-substituted indenes as potential precursors for ansa-zirconocenes

Hagemeister, Timo,Jutzi, Peter,Stammler, Anja,Stammler, Hans-Georg

, p. 1255 - 1262 (2003)

Chiral amino-functionalized silicon-bridged indene derivatives 4a-4c were synthesized from 3-(2-(N,N-dialkylamino)ethyl)indenes 2a-2c. The C-Si coupling reactions are regioselective, leading exclusively to the formation of 1,3-disubstituted isomers in a rac/meso ratio of 1:1, as indicated by NMR spectroscopy. The solid-state structure of the dimethylsilyl-bridged bisindene (R,R)-4a is described. The formation of corresponding ansa-zirconocenes via amine elimination chemistry was monitored by 1H NMR spectroscopy.

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