50551-10-5

Basic information

• Product Name: CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER
• Synonyms: TIMTEC-BB SBB010259;CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER;3-Amino-3-iminopropanoic acid ethyl ester;Propanoic acid, 3-aMino-3-iMino-, ethyl ester
• CAS NO: 50551-10-5
• Molecular Formula: C₅H₁₀N₂O₂
• Molecular Weight: 130.15
• Mol File: 50551-10-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 224℃
• Boiling Point: 197.1 °C at 760 mmHg
• Flash Point: 73 °C
• Appearance: /
• Density: 1.19
• PKA: 10.69±0.40(Predicted)
• CAS DataBase Reference: CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER(50551-10-5)
• EPA Substance Registry System: CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER(50551-10-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 50551-10-5(Hazardous Substances Data)

Usage

General Description

CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER is a chemical compound with the molecular formula C5H10N2O2. It is a carboxylic ester and contains a carbamimidoyl group. CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER may have various industrial or laboratory applications, including its use as a reagent in organic synthesis. It is important to handle and store this compound with caution, as it may have potential hazards and safety considerations associated with its use. Further research and testing may be necessary to fully understand and utilize the properties and potential applications of CARBAMIMIDOYL-ACETIC ACID ETHYL ESTER.

Upstream product

• 64-17-5 ethanol 
• 2318-25-4 ethyl 3-ethoxy-3-iminopropanoate hydrochloride 
• 27317-59-5 Ethyl 3-ethoxy-3-iminopropionate 

Downstream Products

• 161987-77-5 2-Amino-4-phenyl-1,4-dihydro-[1,8]naphthyridine-3-carboxylic acid ethyl ester 
• 873192-75-7 2-amino-5-o-tolyl-1H-pyrrole-3-carboxylic acid ethyl ester 
• 873192-77-9 2-amino-5-(4-methylphenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 173458-96-3 2-amino-3-ethoxycarbonyl-5-(2-methoxy-phenyl)-1H-pyrrole 
• 873192-76-8 2-amino-5-(2-chloro-phenyl)-1H-pyrrole-3-carboxylic acid ethyl ester 
• 173458-92-9 2-amino-3-carboxethyl-5-(4-methoxyphenyl)-pyrrole 
• 187724-98-7 5-amino-1H-pyrrole-2,4-dicarboxylic acid diethyl ester 
• 59155-46-3 2-amino-4-(3-cyano-phenyl)-5-oxo-1,4,5,6,7,8-hexahydro-quinoline-3-carboxylic acid ethyl ester 
• 50551-04-7 2-amino-4-(4,5-dimethoxy-2-nitro-phenyl)-5-oxo-1,4,5,6,7,8-hexahydro-quinoline-3-carboxylic acid ethyl ester 
• 50551-03-6 2-amino-4-(4-nitro-2-trifluoromethyl-phenyl)-5-oxo-1,4,5,6,7,8-hexahydro-quinoline-3-carboxylic acid ethyl ester 
• 50626-60-3 2-amino-6-methyl-4-(3'-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid 3-ethyl ester-5-β-methoxyethyl ester 
• 52157-10-5 2-amino-6-methyl-4-phenyl-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester 
• 1437869-83-4 C₁₉H₁₆Cl₂N₂O₂ 
• 108290-86-4 2-amino-1H-pyrrole-3-carboxylic acid ethyl ester 

Relevant articles and documents

Synthesis and molecular modeling of 1H-pyrrolopyrimidine-2,4-dione derivatives as ligands for the α1-adrenoceptors

Three different series of 1H-pyrrolopyrimidine-2,4-dione derivatives were designed and synthesized as ligands for the α1-adrenergic receptors (α1-ARs). A microwave-assisted protocol was developed in order to improve purity and yields

3-Arylpiperazinylethyl-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione derivatives as novel, high-affinity and selective α1- adrenoceptor ligands

The discovery of a new series of selective and high-affinity α1-adrenoceptor (α1-AR) ligands, characterized by a 1H-pyrrolo[2,3-d]-pyrimidine-2,4(3H,7H)-dione system, is described in this paper. Some synthesized compounds, including 20, 22, and 30, displayed affinity in the nanomolar range for α1-ARs and substantial selectivity with respect to 5-HT1A and dopaminergic D1 and D 2 receptors. Functional assays, performed on selected derivatives, showed antagonistic properties.