773069
Fmoc-N-Me-Cys(Trt)-OH
97% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 944797-51-7
Synonym(S): N-α-Fmoc-N-α-methyl-S-trityl-L-cysteine
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 1 G | 773069-1-G | In Stock | ₹ 44,414.98 |
773069 - 1 G
In Stock
Quantity
1
Base Price: ₹ 44,414.98
GST (18%): ₹ 7,994.696
Total Price: ₹ 52,409.676
Quality Level
100
Assay
97% (HPLC)
form
powder or crystals
optical activity
[α]22/D -25.0°, c = 0.5% in dichloromethane
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
234-239 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
InChI
1S/C38H33NO4S/c1-39(37(42)43-25-34-32-23-13-11-21-30(32)31-22-12-14-24-33(31)34)35(36(40)41)26-44-38(27-15-5-2-6-16-27,28-17-7-3-8-18-28)29-19-9-4-10-20-29/h2-24,34-35H,25-26H2,1H3,(H,40,41)/t35-/m0/s1
Related Products
Description
- Application: Fmoc-N-Me-Cys(Trt)-OH is a Fmoc-protected derivative of N-methyl cysteine used as a building block to prepare peptide thioesters under acidic conditions. The residue attached to the amino group of N-methylcysteine can migrate to the cysteinyl thiol group, resulting in the formation of a peptide thioester. The introduction of this Fmoc-protected derivative is best achieved using HATU as a coupling reagent in the presence of DIPEA (N, N-Diisopropylethylamine). It can also be used to prepare Fmoc-N-Me-Cys(Trt)-OAllyl intermediate for the solid-phase synthesis of dithiol Triostin A.[1]
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Quality Level: 100
Assay: 97% (HPLC)
form: powder or crystals
optical activity: [α]22/D -25.0°, c = 0.5% in dichloromethane
reaction suitability: reaction type: Fmoc solid-phase peptide synthesis
mp: 234-239 °C
application(s): peptide synthesis
functional group: Fmoc
storage temp.: 2-8°C
InChI: 1S/C38H33NO4S/c1-39(37(42)43-25-34-32-23-13-11-21-30(32)31-22-12-14-24-33(31)34)35(36(40)41)26-44-38(27-15-5-2-6-16-27,28-17-7-3-8-18-28)29-19-9-4-10-20-29/h2-24,34-35H,25-26H2,1H3,(H,40,41)/t35-/m0/s1
Quality Level:
100
Assay:
97% (HPLC)
form:
powder or crystals
optical activity:
[α]22/D -25.0°, c = 0.5% in dichloromethane
reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis
mp:
234-239 °C
application(s):
peptide synthesis
functional group:
Fmoc
storage temp.:
2-8°C
InChI:
1S/C38H33NO4S/c1-39(37(42)43-25-34-32-23-13-11-21-30(32)31-22-12-14-24-33(31)34)35(36(40)41)26-44-38(27-15-5-2-6-16-27,28-17-7-3-8-18-28)29-19-9-4-10-20-29/h2-24,34-35H,25-26H2,1H3,(H,40,41)/t35-/m0/s1
Quality Level: 100
Assay: 97%
form: powder or crystals
optical activity: [α]22/D -39.0°, c = 0.5% in DMF
reaction suitability: reaction type: Fmoc solid-phase peptide synthesis
mp: 135-140 °C
application(s): peptide synthesis
functional group: Fmoc
storage temp.: 2-8°C
InChI: __
Quality Level:
100
Assay:
97%
form:
powder or crystals
optical activity:
[α]22/D -39.0°, c = 0.5% in DMF
reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis
mp:
135-140 °C
application(s):
peptide synthesis
functional group:
Fmoc
storage temp.:
2-8°C
InChI:
__
Quality Level: 200
Assay: ≥99.0% (RT)
form: powder or crystals
optical activity: __
reaction suitability: __
mp: 122 °C (lit.)
application(s): __
functional group: __
storage temp.: __
InChI: __
Quality Level:
200
Assay:
≥99.0% (RT)
form:
powder or crystals
optical activity:
__
reaction suitability:
__
mp:
122 °C (lit.)
application(s):
__
functional group:
__
storage temp.:
__
InChI:
__
Quality Level: __
Assay: 97% (HPLC)
form: powder or crystals
optical activity: [α]22/D -14.0°, c = 1% in chloroform
reaction suitability: reaction type: Fmoc solid-phase peptide synthesis
mp: 189-194 °C (decomposition)
application(s): peptide synthesis
functional group: BocFmoc
storage temp.: 2-8°C
InChI: 1S/C27H34N2O6/c1-27(2,3)35-25(32)28-16-10-9-15-23(24(30)31)29(4)26(33)34-17-22-20-13-7-5-11-18(20)19-12-6-8-14-21(19)22/h5-8,11-14,22-23H,9-10,15-17H2,1-4H3,(H,28,32)(H,30,31)/t23-/m0/s1
Quality Level:
__
Assay:
97% (HPLC)
form:
powder or crystals
optical activity:
[α]22/D -14.0°, c = 1% in chloroform
reaction suitability:
reaction type: Fmoc solid-phase peptide synthesis
mp:
189-194 °C (decomposition)
application(s):
peptide synthesis
functional group:
BocFmoc
storage temp.:
2-8°C
InChI:
1S/C27H34N2O6/c1-27(2,3)35-25(32)28-16-10-9-15-23(24(30)31)29(4)26(33)34-17-22-20-13-7-5-11-18(20)19-12-6-8-14-21(19)22/h5-8,11-14,22-23H,9-10,15-17H2,1-4H3,(H,28,32)(H,30,31)/t23-/m0/s1