ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >α-Amino acid >D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid

D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid

D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Structure
CAS No.
103733-65-9
Chemical Name:
D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
Synonyms
D-TIC;H-D-TIC-OH;RARECHEM BK PT 0079;Icatibant Impurity 4;D-PHENYLALANINE ANALOGUE;D-1,2,3,4-Tetrahydroisoquinoline;Tetrahydroisoquinoline-3-carboxylic acid;D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID;1,2,3,4-D-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID;1,2,3,4-TETRAHYDROISOQUINOLINE-(3R)-CARBOXYLIC ACID
CBNumber:
CB7397017
Molecular Formula:
C10H11NO2
Molecular Weight:
177.2
MOL File:
103733-65-9.mol
MSDS File:
SDS
Modify Date:
2023/9/12 11:00:47

D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Properties

Melting point 320-323 °C (decomp)
Boiling point 372.0±42.0 °C(Predicted)
Density 1.225±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Aqueous Acid (Slightly), Aqueous Base (Sparingly, Sonicated)
pka 2.21±0.20(Predicted)
form Crystalline Powder
color White
InChI InChI=1S/C10H11NO2/c12-10(13)9-5-7-3-1-2-4-8(7)6-11-9/h1-4,9,11H,5-6H2,(H,12,13)/t9-/m1/s1
InChIKey BWKMGYQJPOAASG-SECBINFHSA-N
SMILES C1C2=C(C=CC=C2)C[C@H](C(O)=O)N1
CAS DataBase Reference 103733-65-9(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29334900
NFPA 704
0
2 0

D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Chemical Properties,Uses,Production

Description

D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid ((3R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid) is a magnetic, neutral compound. It is used as a pharmacological study to investigate the reaction mechanism and kinetics of the deuteration process. The asymmetric synthesis of D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid has been investigated using vinylene chloride and hydantoin as reactants. There are various parameters that affect the kinetics of this reaction such as solvent type and temperature. The nitric oxide synthase inhibitor activity of D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid has been studied in vitro. Results have shown that it inhibits nitric oxide synthase by binding to the heme iron of the enzyme and preventing the conversion of arginine

Chemical Properties

White solid

Uses

(R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.

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D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Spectrum

(3R)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid (R)-1,2,3,4-Tetrahydro-isoquinolin-3-carboxylic acid H-D-Tic-OH D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (3R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid≥ 99% (assay) (R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acid,99%e.e. 1,2,3,4-TETRAHYDROISOQUINOLINE-(3R)-CARBOXYLIC ACID 1,2,3,4-D-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID 3-ISOQUINOLINECARBOXYLIC ACID, 1,2,3,4-TETRAHYDRO-, (3R)- (3R)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID H-D-TIC-OH D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID D-[3R]-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID D-TIC (R)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID (R)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID RARECHEM BK PT 0079 D-1,2,3,4-Tetrahydroisoquinoline (R)-1,2,3,4-Tetrahydro-3-Isoquinoliceearboxylic Acid D-PHENYLALANINE ANALOGUE Tetrahydroisoquinoline-3-carboxylic acid (R)-(+)-1,2,3,4-Tetrahydroisoquinoline-3-CarboxylicAci D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid USP/EP/BP 103733-65-9 D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Icatibant Impurity 4 103733-65-9 Others Peptide Synthesis Specialty Synthesis Unnatural Amino Acid Derivatives a-amino Others Peptide Synthesis Unnatural Amino Acid Derivatives Amino Acids