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Diethyl 4-amino-2,5-dihydro-1H-pyrrole-1,3-dicarboxylate is a chemical compound with the molecular formula C10H16N2O4. It is a derivative of pyrrole, a heterocyclic organic compound consisting of a five-membered ring with one nitrogen atom and four carbon atoms. This specific compound features an amino group (-NH2) at the 4-position, and two ester groups (-COOCH2CH3) at the 1 and 3 positions, which are derived from diethyl. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. Its chemical structure and reactivity make it a valuable building block in organic chemistry, allowing for the creation of a wide range of complex molecules.

1212-06-2

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1212-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1212-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1212-06:
(6*1)+(5*2)+(4*1)+(3*2)+(2*0)+(1*6)=32
32 % 10 = 2
So 1212-06-2 is a valid CAS Registry Number.

1212-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 4-amino-2,5-dihydropyrrole-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 4-amino-2,5-dihydro-pyrrole-1,3-dicarboxylic acid diethyl ester

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:1212-06-2 SDS

1212-06-2Downstream Products

1212-06-2Relevant academic research and scientific papers

Enantioselective hydrogenation of tetrasubstituted olefins of cyclic β-(acylamino)acrylates

Tang, Wenjun,Wu, Shulin,Zhang, Xumu

, p. 9570 - 9571 (2007/10/03)

Hydrogenation of a series of cyclic β-(acylamino)acrylates with tetrasubstituted olefins has been accomplished successfully with the use of Ru catalysts with chiral biaryl ligands such as C3-TunaPhos, and up to over 99% ee's have been achieved. This methodology provides an efficient catalytic method for the synthesis of both cis and trans chiral cyclic β-amino acid derivatives. Copyright

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