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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
advtechind fmoc-L-propargylglycine, 97%
on request
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
capotchem Fmoc-l-propargylglycine, 98%(Min,HPLC)
on request
chemieliva Fmoc-Pra-OH, 98%
5G
10G
20G
50G
100G
50KG
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
glbiochem (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pent-4-ynoic acid, 98%
on request
manchesterorganics (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid
bocsci Fmoc-L-propargylglycine, ≥ 99.5% (Chiral HPLC)
on request
chempur FMOC-L-propargylglycine/ >97%
1 g
and other units
chempur Fmoc-propargyl-Gly-OH / min. 98.0%
1 g
and other units
chempur Fmoc-L-propargylglycine/ 98%
1 g
and other units
001chemical Fmoc-Pra-OH, NLT 98%
on request
hairuichem Fmoc-L-propargylglycine, 98%NLT
on request
activate-scientific Fmoc-(S)-2-Propargylglycine, 98% ee
25.0g
1.0g
5.0g
chempur Fmoc-Pra-OH/ 98%
100 g
and other units

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