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(S)-N-Fmoc-Propargylglycine
(S)-N-(9-Fluorenylmethoxycarbonyl)-2-amino-4-pentynoic acid
Fmoc-L-propargylglycine
Fmoc-L-Pra-OH
Predict NMR spectrum
RN: 
198561-07-8
MF: 
C20H17NO4
MW: 
335.35928
mp (°C): 
175
InChI:  1S/C20H17NO4/c1-2-7-18(19(22)23)21-20(24)25-12-17-15-10-5-3-8-13(15)14-9-4-6-11-16(14)17/h1,3-6,8-11,17-18H,7,12H2,(H,21,24)(H,22,23)/t18-/m0/s1
InChIKey:  DJGMNCKHNMRKFM-SFHVURJKSA-N
H donor:  2
H acceptor:  5
Rotatable bond:  6
Stereocenter:  1
cLogP:  2.601
cLogS:  -5.097
Polar surface:  75.63
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  Supplier     Description     Reference  
bocsci Fmoc-L-propargylglycine, ≥ 99.5% (Chiral HPLC)
on request
amadischem Fmoc-Pra-OH, 98%
Bulk, semi-bulk
capotchem Fmoc-l-propargylglycine, 98%(Min,HPLC)
100kg
200kg
tons
1kg
5kg
25kg
advtechind fmoc-L-propargylglycine, 97%
1G
leapchem fmoc-L-propargylglycine
on request
leapchem fmoc-L-propargylglycine
on request
alfa-chemistry Building block for the introduction by Fmoc SPPS. of an amino acid bearing an alkyne side chain. Such derivatives are useful tools for the synthesis of cyclic peptides by an alkyne-alkyne Glaser coupling, involving Cu(OAc)2/pyridine and heating to 60 ℃using microwaves.
1g
5g
10g
25g
100g
250g
aifchem Fmoc-Pra-OH, 98%
5g
10g
25g
chemcube
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)pent-4-ynoic acid
Fmoc-L-Propargylglycine
Fmoc-Pra-OH
 , >98%
on request
oakwood
Fmoc-L-propargylglycine
250mg
1g
5g
yuansu-reagent FMOC-L-PROPARGYLGLYCINE
rovathin
Fmoc-L-Propargylglycine
 , 95%
on request
manchesterorganics (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid
aboundchem Fmoc-L-Propargylglycine, 98%
1g
5g
25g
galedo-bio Fmoc-L-Propargylglycine, Extremely high
Gram quantities
bocsci Fmoc-L-propargylglycine, ≥ 99.5% (Chiral HPLC)
on request
chempur Fmoc-Pra-OH/ 98%
100 g
and other units
ivychem 4-Pentynoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2S)-
on request
chempur Fmoc-propargyl-Gly-OH / min. 98.0%
1 g
and other units
iris-biotech Fmoc-L-Pra-OH
FAA1589.0001 1 g
FAA1589.0005 5 g
FAA1589.0025 25 g

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