15912-55-7

Basic information

• Product Name: 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
• Synonyms: 1-ethyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylate;(3S)-ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate;3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-, ethyl ester, (3S)-
• CAS NO: 15912-55-7
• Molecular Formula: C₁₂H₁₅NO₂
• Molecular Weight: 205.25
• EINECS: 255-273-0
• Mol File: 15912-55-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 378.7°C at 760 mmHg
• Flash Point: 182.8°C
• Appearance: /
• Vapor Pressure: 2.07E-06mmHg at 25°C
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER(15912-55-7)
• EPA Substance Registry System: 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER(15912-55-7)

Safety Data

• Hazardous Substances Data: 15912-55-7(Hazardous Substances Data)

Usage

General Description

1,2,3,4-Tetrahydro-Isoquinoline-3-Carboxylic Acid Ethyl Ester, also known as Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate, is a chemical compound falling under the category of Isoquinoline carboxylic acids and derivatives. This organic compound commonly consists of atoms of hydrogen, carbon, oxygen, and nitrogen. 1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is known for its heterocyclic ring, a feature that is common with the ester derivatives of isoquinoline. However, not much information is available about it as it is an extremely rare compound. The molecule also possesses ester functional groups, which are characterized by the carbon-oxygen double bond and an oxygen single bond.

InChI:InChI=1/C12H15NO2/c1-2-10-9-6-4-3-5-8(9)7-11(13-10)12(14)15/h3-6,10-11,13H,2,7H2,1H3,(H,14,15)/p-1

Upstream product

• 64-17-5 ethanol 
• 74163-81-8 L-Tic-OH 
• 67123-97-1 (R,S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid 

Downstream Products

• 18881-17-9 (S)-3-hydroxymethyl-1,2,3,4-tetrahydroisoquinoline 
• 1254944-66-5 ethyl 2-(5-(methylthio)thiophene-2-carbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate 
• 66937-37-9 2-[N2-(6,7-dimethoxy-2-naphthalenesulfonyl)-L-arginyl]-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid 
• 74163-81-8 L-Tic-OH 
• 88106-00-7 N-<4-(4-hydroxyphenyl)butyryl>-L-3-carbethoxy-1,2,3,4-tetrahydro-2H-isoquinoline 
• 63006-93-9 3-hydroxymethyl-1,2,3,4-tetrahydroisoquinoline 
• 1380547-82-9 3-ethyl 2-(3-(trifluoromethyl)phenyl) 3,4-dihydroisoquinoline-2,3(1H)-dicarboxylate 
• 1262842-13-6 C₁₉H₂₁NO₄S 
• 1380547-84-1 3-ethyl 2-phenyl 3,4-dihydroisoquinoline-2,3(1H)-dicarboxylate 
• 101195-64-6 ethyl 2-(phenylcarbamoyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate 
• 1380547-77-2 C₁₉H₁₈ClNO₃ 
• 1380547-80-7 C₁₈H₁₈BrNO₄S 
• 1380548-02-6 C₃₁H₃₁NO₃ 
• 1380547-98-7 (3-(([1,1'-biphenyl]-4-yloxy)methyl)-3,4-dihydroisoquinolin-2(1H)-yl)(naphthalen-1-yl)methanone 

Relevant articles and documents

Chiral tricarbonyl(η6-arene)chromium complexed diphosphanes. Highly enantioselective rhodium-mediated hydrogenation of ketones

Arenechromium complexed diastereomeric aminophosphine-phosphinite ligands derived from tetrahydroisoquinoline have been synthesised and examined as chiral auxiliaries in the hydrogenation of functionalised ketones. A cyclopentyl-substituted anti-stereoisomer is providing the highest enantioselectivities (up to >99% ee).

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An organogel formed from a cyclic β-aminoalcohol

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