F5312
Fmoc-(R)-propargyl-Ala-OH
Manufacturer: Sigma Aldrich
CAS Number: 1198791-65-9
Synonym(S): (R)-N-Fmoc-α-propargyl-Ala-OH, (R)-N-Fmoc-α-propargylalanine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | F5312-1-G | In Stock | ₹ 47,099.58 |
F5312 - 1 G
In Stock
Quantity
1
Base Price: ₹ 47,099.58
GST (18%): ₹ 8,477.924
Total Price: ₹ 55,577.504
Quality Level
200
reaction suitability
reaction type: click chemistry
application(s)
peptide synthesis
functional group
Fmoc
shipped in
wet ice
storage temp.
−20°C
SMILES string
O=C(N[C@](C)(CC#C)C(O)=O)OCC1C2=CC=CC=C2C3=C1C=CC=C3
InChI
1S/C21H19NO4/c1-3-12-21(2,19(23)24)22-20(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h1,4-11,18H,12-13H2,2H3,(H,22,25)(H,23,24)/t21-/m1/s1
InChI key
ZXOKSWZUJXKQCQ-OAQYLSRUSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-alpha-Me-D-Gly(Propargyl)-OH | 1198791-65-9, 50GR | STA PHARMACEUTICAL US LLC | ₹ 4,02,931.13 | |
| | STA PHARMACEUTICAL US LLC WuXi TIDES Fmoc-alpha-Me-D-Gly(Propargyl)-OH | 1198791-65-9, 5GR | STA PHARMACEUTICAL US LLC | ₹ 63,605.30 | |
 | (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpent-4-ynoic acid | ChemScene | ₹ 6,673.68 - ₹ 1,13,195.88 | |
 | 1198791-65-9 | (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpent-4-ynoic acid | A2B Chem | ₹ 7,358.16 - ₹ 1,13,195.88 |
Related Products
Description
- Application: Alkyne amino acid, more stable for peptide stapling via click chemistry than propargylglycine.
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Quality Level: 200
reaction suitability: reaction type: click chemistry
application(s): peptide synthesis
functional group: Fmoc
shipped in: wet ice
storage temp.: −20°C
SMILES string: O=C(N[C@](C)(CC#C)C(O)=O)OCC1C2=CC=CC=C2C3=C1C=CC=C3
InChI: 1S/C21H19NO4/c1-3-12-21(2,19(23)24)22-20(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h1,4-11,18H,12-13H2,2H3,(H,22,25)(H,23,24)/t21-/m1/s1
InChI key: ZXOKSWZUJXKQCQ-OAQYLSRUSA-N
Quality Level:
200
reaction suitability:
reaction type: click chemistry
application(s):
peptide synthesis
functional group:
Fmoc
shipped in:
wet ice
storage temp.:
−20°C
SMILES string:
O=C(N[C@](C)(CC#C)C(O)=O)OCC1C2=CC=CC=C2C3=C1C=CC=C3
InChI:
1S/C21H19NO4/c1-3-12-21(2,19(23)24)22-20(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h1,4-11,18H,12-13H2,2H3,(H,22,25)(H,23,24)/t21-/m1/s1
InChI key:
ZXOKSWZUJXKQCQ-OAQYLSRUSA-N
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