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Pyrrolidine, 3-ethenyl-4-methylene-1-(trifluoroacetyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153391-89-0

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153391-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153391-89-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,9 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153391-89:
(8*1)+(7*5)+(6*3)+(5*3)+(4*9)+(3*1)+(2*8)+(1*9)=140
140 % 10 = 0
So 153391-89-0 is a valid CAS Registry Number.

153391-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-ethenyl-4-methylidenepyrrolidin-1-yl)-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names 3-ETHENYL-4-METHYLENE-1-(TRIFLUOROACETYL)-PYRROLIDINE

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:153391-89-0 SDS

153391-89-0Upstream product

153391-89-0Downstream Products

153391-89-0Relevant academic research and scientific papers

Rhodium(I)-Ctalyzed 'Metallo-Ene' Cyclizations/β-Eliminations

Oppolzer, Wolfgang,Fuerstner, Alois

, p. 2329 - 2337 (2007/10/02)

Octadienyl carbonates 5 provide cyclic 1,4-dienes 6 when treated with RhI complexes (1-10 mol-percent) at 80 deg C.Similar cyclization of cyclohexenyl acetate 8 affords cis-fused hexahydroindene 9.Analogues ring closures of nonadiene carbonate 10 yield preferably the cis-divinylpyrrolidine 11 with RhI catalysis but the trans-isomer 12 when catalyzed by Pd0.Azaoctadienyl carbonate 5a undergoes elimination with (5 mol-percent, 80 deg C) in MeCN giving acyclic triene 7.

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