129223-22-9
- Product Name：Fmoc-Pro-Pro-OH
- Molecular Formula：C25H26N2O5
- Purity：99%
- Molecular Weight：434.492
Product Details;
CasNo： 129223-22-9
Molecular Formula： C25H26N2O5
Quality Factory Sells Top Purity 99% Fmoc-Pro-Pro-OH 129223-22-9 with Safe Delivery
- Molecular Formula:C25H26N2O5
- Molecular Weight:434.492
- Vapor Pressure:0mmHg at 25°C
- Refractive Index:1.638
- Boiling Point:677.731 °C at 760 mmHg
- PKA:3.51±0.20(Predicted)
- Flash Point:363.679 °C
- PSA：87.15000
- Density:1.353 g/cm3
- LogP:3.35130
Fmoc-Pro-Pro-OH(Cas 129223-22-9) Usage
|
General Description |
Fmoc-Pro-Pro-OH, also known as Fmoc-Dipropylglycine, is a chemical compound used in the field of peptide synthesis. Fmoc-Pro-Pro-OH is utilized in the synthesis of different types of peptides, including those that play crucial roles in various biological processes. The "Fmoc" part of the name refers to the fluorenylmethyloxycarbonyl protecting group which is attached to the amino group of the proline. It serves to shield reactive sites in the amino acid and allows for selective chemical reactions during peptide synthesis. The "Pro-Pro" refers to the two proline residues, and "OH" denotes the presence of a hydroxyl group. |
InChI:InChI=1/C25H26N2O5/c28-23(26-13-6-12-22(26)24(29)30)21-11-5-14-27(21)25(31)32-15-20-18-9-3-1-7-16(18)17-8-2-4-10-19(17)20/h1-4,7-10,20-22H,5-6,11-15H2,(H,29,30)/t21-,22-/m0/s1
129223-22-9 Relevant articles
3-Azaspiro[5,5]undecan-2,4-dioxo-3-yl diphenyl phosphate (ASUD-diphenyl phosphate), a new reagent for the synthesis of the N-protected amino acid-ASUD ester
Rao, B. Leelamaheswara,Nowshuddin, Shaik,Jha, Anjali,Divi, Murali K.,Rao
, p. 487 - 491 (2016/06/06)
A new reagent, 3-azaspiro[5,5]undecan-2,...
Solution-phase synthesis and evaluation of tetraproline chiral stationary phases
Dai, Zhi,Ye, Guozhong,Pittman Jr., Charles U.,Li, Tingyu
experimental part, p. 329 - 338 (2012/05/20)
A protocol was developed for the solutio...
Functional identification and structure determination of two novel prolidases from cog1228 in the amidohydrolase superfamily
Xiang, Dao Feng,Patskovsky, Yury,Xu, Chengfu,Fedorov, Alexander A.,Fedorov, Elena V.,Sisco, Abby A.,Sauder, J. Michael,Burley, Stephen K.,Almo, Steven C.,Raushel, Frank M.
experimental part, p. 6791 - 6803 (2011/05/05)
Two uncharacterized enzymes from the ami...
Fmoc-peptide acid chlorides : Preparation, characterization and utility in peptide synthesis
Gayathri,Gopi,Suresh Babu
, p. 151 - 154 (2007/10/03)
Fmoc-protected peptide acid chlorides ha...
129223-22-9 Process route
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-
C30H32N2O6
-
-
147-85-3,25191-13-3,37159-97-0,4305-67-3,4607-28-7
L-proline
-
-
129223-22-9
Fmoc-L-Pro-Pro-OH
| Conditions | Yield |
|---|---|
|
With
triethylamine;
In
tetrahydrofuran;
at 20 ℃;
for 15h;
|
91% |
-
-
1366733-84-7
Fmoc-Pro-Pro-O-t-butyl ester
-
-
129223-22-9
Fmoc-L-Pro-Pro-OH
| Conditions | Yield |
|---|---|
|
With
trifluoroacetic acid;
In
dichloromethane;
at 20 ℃;
for 6h;
|
98.9% |
129223-22-9 Upstream products
-
209910-36-1
Fmoc-Pro-Pro-OMe
-
115134-39-9
(S)-(9H-fluoren-9-yl)methyl 2-carbamoylpyrrolidine-1-carboxylate
-
1366733-84-7
Fmoc-Pro-Pro-O-t-butyl ester
-
71989-31-6
Fmoc-Pro-OH
129223-22-9 Downstream products
-
134303-96-1
Fmoc-Pro-Pro-Pro-OH
-
20488-28-2
L-prolyl-L-proline
-
1366733-85-8
Fmoc-Pro-Pro-O-pentafluorophenyl ester
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-
Fmoc-Pro-Pro-Pro-OH
CAS：134303-96-1
