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47595

Sigma-Aldrich

Fmoc-Sar-OH

≥98.0%

Synonym(s):

Fmoc-N-methylglycine, Fmoc-sarcosine

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About This Item

Empirical Formula (Hill Notation):
C18H17NO4
CAS Number:
77128-70-2
Molecular Weight:
311.33
Beilstein/REAXYS Number:
6660958
MDL number:
MFCD00151926
UNSPSC Code:
12352209
PubChem Substance ID:
57651028
NACRES:
NA.26

assay

≥98.0%

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CN(CC(O)=O)C(=O)OCC1c2ccccc2-c3ccccc13

InChI

1S/C18H17NO4/c1-19(10-17(20)21)18(22)23-11-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,16H,10-11H2,1H3,(H,20,21)

InChI key

ZHKQIADIIYMFOZ-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Tatsuhiko Kondo et al.
Plant & cell physiology, 52(1), 30-36 (2010-10-12)
CLAVATA3 (CLV3) is a plant peptide hormone in which the proline residues are post-translationally hydroxylated and glycosylated. CLV3 plays a key role in controlling the stem cell mass in the shoot meristem of Arabidopsis thaliana. In a previous report, we
Ewa Radzikowska et al.
Organic & biomolecular chemistry, 13(1), 269-276 (2014-11-05)
Chimeric oligonucleotides containing phosphodiester and phosphorothioate linkages have been obtained using the solid phase synthesis. The oligonucleotide parts possessing natural internucleotide phosphate bonds were assembled using commercially available nucleoside 3'-O-(2-cyanoethyl-N,N-diisopropylamino)phosphoramidites 7 whereas the phosphorothioate segment was built using nucleoside 3'-O-(2-thio-1,3,2-oxathiaphospholanes)

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