Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L-alanine
≥95% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 2120095-23-8
Synonym(S): (S)-3-(3,4-Bis(trifluoromethyl)phenyl)-2-(tert-butoxycarbonylamino)propanoic acid
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | ALD00348-1-G | In Stock | ₹ 13,336.40 |
ALD00348 - 1 G
In Stock
Quantity
1
Base Price: ₹ 13,336.40
GST (18%): ₹ 2,400.552
Total Price: ₹ 15,736.952
description
ALPH: +24.0, 0.5%EtOH
Quality Level
100
Assay
≥95% (HPLC)
form
powder or solid
reaction suitability
reaction type: Boc solid-phase peptide synthesisreagent type: ligandreaction type: C-H Activation
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC(C(F)(F)F)=C(C(F)(F)F)C=C1)=O
InChI
1S/C16H17F6NO4/c1-14(2,3)27-13(26)23-11(12(24)25)7-8-4-5-9(15(17,18)19)10(6-8)16(20,21)22/h4-6,11H,7H2,1-3H3,(H,23,26)(H,24,25)/t11-/m0/s1
InChI key
LLRXWQAYIGATCH-NSHDSACASA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L-alanine | ChemScene | -- |
Related Products
Description
- Application: Unnatural amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).
- Other Notes: Ligand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids
SAFETY INFORMATION
Pictograms
Signal Word
Warning
Hazard Statements
Precautionary Statements
P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Compare Similar Items
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description: ALPH: +24.0, 0.5%EtOH
Quality Level: 100
Assay: ≥95% (HPLC)
form: powder or solid
reaction suitability: reaction type: Boc solid-phase peptide synthesisreagent type: ligandreaction type: C-H Activation
application(s): peptide synthesis
storage temp.: 2-8°C
SMILES string: OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC(C(F)(F)F)=C(C(F)(F)F)C=C1)=O
InChI: 1S/C16H17F6NO4/c1-14(2,3)27-13(26)23-11(12(24)25)7-8-4-5-9(15(17,18)19)10(6-8)16(20,21)22/h4-6,11H,7H2,1-3H3,(H,23,26)(H,24,25)/t11-/m0/s1
InChI key: LLRXWQAYIGATCH-NSHDSACASA-N
description: __
Quality Level: 100
Assay: 95% (HPLC)
form: solid
reaction suitability: reaction type: solution phase peptide synthesis
application(s): peptide synthesis
storage temp.: 2-8°C
SMILES string: OC([C@@H](NC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)CC4=CC=CC=C4OC)=O
InChI: 1S/C25H23NO5/c1-30-23-13-7-2-8-16(23)14-22(24(27)28)26-25(29)31-15-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-13,21-22H,14-15H2,1H3,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key: CBCSNZJHURMDMO-QFIPXVFZSA-N
description: __
Quality Level: 100
Assay: 95% (HPLC)
form: solid
reaction suitability: reaction type: solution phase peptide synthesis
application(s): peptide synthesis
storage temp.: 2-8°C
SMILES string: OC([C@@H](NC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)CC4=CC=CC=C4OC)=O
InChI: 1S/C25H23NO5/c1-30-23-13-7-2-8-16(23)14-22(24(27)28)26-25(29)31-15-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-13,21-22H,14-15H2,1H3,(H,26,29)(H,27,28)/t22-/m0/s1
InChI key: CBCSNZJHURMDMO-QFIPXVFZSA-N
