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1H-Pyrrolizin-1-amine,hexahydro-2-(1-methylethyl)-,(1R,2R,7aR)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

389621-34-5

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  • 1H-Pyrrolizin-1-amine,hexahydro-2-(1-methylethyl)-,(1R,2R,7aR)-(9CI)

    Cas No: 389621-34-5

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389621-34-5 Usage

Structure

Bicyclic amine with a pyrrolizine ring

Usage

Building block in organic synthesis and pharmaceutical research

Chemical properties

Of interest to researchers in drug development and other fields of chemistry

Potential uses

Not specified in the provided material

Check Digit Verification of cas no

The CAS Registry Mumber 389621-34-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,6,2 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 389621-34:
(8*3)+(7*8)+(6*9)+(5*6)+(4*2)+(3*1)+(2*3)+(1*4)=185
185 % 10 = 5
So 389621-34-5 is a valid CAS Registry Number.

389621-34-5SDS

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 1H-Pyrrolizin-1-amine,hexahydro-2-(1-methylethyl)-,(1R,2R,7aR)-(9CI)

1.2 Other means of identification

Product number -
Other names -

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:389621-34-5 SDS

389621-34-5Downstream Products

389621-34-5Relevant articles and documents

Regiochemical aspects of intramolecular cycloadditions of nitrones derived from N-(2-alkenyl)-2-pyrrolecarbaldehydes. Competitive entries to pyrrolizidine and indolizidine derivatives

Broggini, Gianluigi,La Rosa, Concetta,Pilati, Tullio,Terraneo, Alberto,Zecchi, Gaetano

, p. 8323 - 8332 (2007/10/03)

Intramolecular cycloadditions of unsaturated nitrones derived from a series of N-(2-alkenyl)-2-pyrrolecarbaldehydes (2) have been systematically studied. A pronounced substituent effect has been observed as far as the competitive formation of fused- and bridged-ring regioisomers are concerned. Further elaboration of the two kinds of cycloadducts has given pyrrolizidine and indolizidine derivatives, respectively.

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