- D-Tic-OH
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- $0.00 / 1kg
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2024-04-30
- CAS:103733-65-9
- Min. Order: 1kg
- Purity: 98%;99%
- Supply Ability: 1T+
- D-TIC
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- $1.00 / 1g
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2020-01-06
- CAS:103733-65-9
- Min. Order: 1g
- Purity: 98%
- Supply Ability: 100KG
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| | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Basic information |
| Product Name: | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid | | Synonyms: | (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)- | | CAS: | 103733-65-9 | | MF: | C10H11NO2 | | MW: | 177.2 | | EINECS: | 266-580-4 | | Product Categories: | a-amino;Others;Peptide Synthesis;Unnatural Amino Acid Derivatives;Amino Acids | | Mol File: | 103733-65-9.mol |  |
| | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Chemical 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) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | HS Code | 29334900 |
| | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Usage And Synthesis |
| 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. | | Definition | ChEBI: D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid is a member of isoquinolines. |
| | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Preparation Products And Raw materials |
| Raw materials | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid-->N-(Diphenylmethylene)glycerine tert-butyl ester-->1,2-Bis(bromomethyl)benzene-->Isobutylene | | Preparation Products | D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid-->(R)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID METHYL ESTER |
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