N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
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- CAS-Nr.
- 130309-33-0
- Englisch Name:
- N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
- Synonyma:
- FMOC-D-TIC;FMOC-D-TIQ;FMOC-D-TIC-OH;RARECHEM BK PT 0081;N-ALPHA-(9-FLUORENYLMETHOXYCA;Fmoc-D-Tetrahydroisoquinoline-3-COO;N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-Tic-OH;FMOC-D-TETRAHYDROISOQUINOLINE-1-CARBOXYLIC ACID;FMOC-D-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- CBNumber:
- CB5772674
- Summenformel:
- C25H21NO4
- Molgewicht:
- 399.44
- MOL-Datei:
- 130309-33-0.mol
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N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Eigenschaften
- Schmelzpunkt:
- 160-164 °C
- Siedepunkt:
- 522.37°C (rough estimate)
- Dichte
- 1.2390 (rough estimate)
- Brechungsindex
- 1.6000 (estimate)
- storage temp.
- Sealed in dry,Store in freezer, under -20°C
- Löslichkeit
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- Aggregatzustand
- Powder
- pka
- 3.82±0.20(Predicted)
- InChIKey
- LIRBCUNCXDZOOU-HSZRJFAPSA-N
- CAS Datenbank
- 130309-33-0(CAS DataBase Reference)
N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Chemische Eigenschaften,Einsatz,Produktion Methoden
S-Sätze Betriebsanweisung:
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
white crystalline powder
Verwenden
Fmoc-D-Tic-OH, is an amino acid derivative used in peptide chemistry.
N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 198)Lieferanten
130309-33-0()Verwandte Suche:
- FMOC-(3R)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (R)-N-FMOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (R)-(-)-2-(9-FLUORENYLMETHOXYCARBONYL)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID
- RARECHEM BK PT 0081
- N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-FMOC-D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-1-FMOC-D-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID
- Fmoc-(3R)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid≥ 99% (HPLC)
- FMOC-1,2,3,4-D-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- FMOC-D-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- FMOC-D-[3R]-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- FMOC-D-TETRAHYDROISOQUINOLINE-1-CARBOXYLIC ACID
- FMOC-D-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- FMOC-D-TIC
- FMOC-D-TIC-OH
- FMOC-D-TIQ
- FMOC-(R)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (R)-N-FMOC-1,2,3,4-TETRAHYDROISOQUINO-LI NE-3-CARBOXYLIC AC
- FMOC-D-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID
- N-alpha-(9-Fluorenylmethyloxycarbonyl)-D-1,2,3,4-Tetrahydroisoquinoline
- (R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-FMOC protected
- (R)-2-(((9H-fluoren-9-yl)methoxy)carbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
- N-FMOC-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid,98%
- N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline
- Fmoc-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic
- Fmoc-D-Tetrahydroisoquinoline-3-COO
- FMoc-D-Tic-OH(FMoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid)
- (3R)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-FMOC protected
- Fmoc-D-Tic-OH, (3R)-2-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
- (9H-Fluoren-9-yl)MethOxy]Carbonyl D-Tic-OH
- N-ALPHA-(9-FLUORENYLMETHOXYCA
- (3R)-2-{[(9H-fluoren-9-yl)methoxy]carbonyl}-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
- 2,3(1H)-Isoquinolinedicarboxylic acid, 3,4-dihydro-, 2-(9H-fluoren-9-ylmethyl) ester, (3R)-
- (R)-(-)-2-(9-Fluorenylmethoxycarbonyl)-1,2,3,4-Tetrahydro-3-IsoquinolinecarboxylicAci
- N-Fmoc-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid USP/EP/BP
- (3R)-2-(9H-fluoren-9-ylmethoxycarbonyl)-3,4-dihydro-1H-isoquinoline-3-carboxylic acid
- 130309-33-0
- C25H21NO4
- Specialty Synthesis
- Others
- Peptide Synthesis
- Unnatural Amino Acid Derivatives
- a-amino
- chiral
- Amino Acids
