BOC-TIC-OH
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- CAS-Nr.
- 78879-20-6
- Englisch Name:
- BOC-TIC-OH
- Synonyma:
- Boc-Tic;BOC-L-TIC;BOC-TIC-OH;BOC-L-TIC-OH;Boc-Tic-OH, >=98%;RARECHEM BK PT 0083;BOC-TIC-OH USP/EP/BP;Boc-Tic-OH >=97.0% (TLC);(Tert-Butoxy)Carbonyl Tic-OH;Boc-L-Tetrahydroisoquinoline-3-COOH
- CBNumber:
- CB4750051
- Summenformel:
- C15H19NO4
- Molgewicht:
- 277.32
- MOL-Datei:
- 78879-20-6.mol
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BOC-TIC-OH Eigenschaften
- Schmelzpunkt:
- 125-126.5 °C
- Siedepunkt:
- 420.18°C (rough estimate)
- Dichte
- 1.1311 (rough estimate)
- Brechungsindex
- 1.5080 (estimate)
- storage temp.
- Sealed in dry,2-8°C
- Löslichkeit
- soluble in Methanol
- Aggregatzustand
- Solid
- pka
- 3.88±0.20(Predicted)
- Farbe
- White to off-white
- Optische Aktivität
- [α]20/D +19.0±1.5°, c = 0.7% in methanol
- BRN
- 4297114
BOC-TIC-OH Chemische Eigenschaften,Einsatz,Produktion Methoden
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
Chemische Eigenschaften
white to light beige powder
BOC-TIC-OH Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
BOC-TIC-OH Anbieter Lieferant Produzent Hersteller Vertrieb Händler.
Global( 217)Lieferanten
78879-20-6()Verwandte Suche:
- Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid98+%
- (S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic A
cid,99%e.e.
- N-T-BUTOXYCARBONYL-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (S)-()-N-BOC-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID
- (S)-(+)-N-BOC-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID
- (S)-N-BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- RARECHEM BK PT 0083
- (S)-2-BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (S)-(+)-2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID
- (S)-3,4-DIHYDRO-1H-ISOQUINOLINE-2,3-DICARBOXYLIC ACID 2-TERT-BUTYL ESTER
- BOC-1,2,3,4-L-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- BOC-(3S)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- Boc-Tic-OH >=97.0% (TLC)
- Boc-Tic-OH, >=98%
- BOC-L-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- BOC-L-TIC
- BOC-L-TIC-OH
- BOC-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- BOC-TIC-OH
- BOC-(S)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- 2,3(1H)-ISOQUINOLINEDICARBOXYLIC ACID, 3,4-DIHYDRO-,2-(1,1-DIMETHYLETHYL) ESTER, (3S)-
- (3S)-2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- (S)-(+)-2-(Tertutoxycarbonyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid
- (S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-BOC protected
- (S)-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
- N-T-BUTYLOXYCARBONYL-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-BOC-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid,99%
- Boc-(S)-1,2,3,4-tetrahydroisoquinoline-line-3-carboxylic acid
- N-1-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID
- N-1-T-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID
- N-ALPHA-T-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID
- N-BOC-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-TERT-BUTYLOXYCARBONYL-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID
- N-Boc-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxyli
- N-T-boc-L-1,2,3,4-tetrahydroiso-*quinoline-3-carb
- Boc-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic
- (3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-BOC protected
- Boc-L-Tetrahydroisoquinoline-3-COOH
- Boc-Tic-OH(Boc-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid)
- N-Boc-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxyli acid
- (Tert-Butoxy)Carbonyl Tic-OH
- Boc-Tic
- N-Boc-(S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 98%
- (3S)-2-[(2-methylpropan-2-yl)oxy-oxomethyl]-3,4-dihydro-1H-isoquinoline-3-carboxylate
- N-tert-Butoxycarbonyl-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
- Boc-(S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylicaci
- BOC-TIC-OH USP/EP/BP
- 78879-20-6
- 78879-20-9
- 78879-20-8
- 78879-20-7
- C15H19NO4
- Peptide Synthesis
- Others
- Unnatural Amino Acid Derivatives
- Specialty Synthesis
- a-amino
