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38784

Sigma-Aldrich

4-[(2,4-Dimethoxyphenyl)(Fmoc-amino)methyl]phenoxyacetic acid

≥99.0% (HPLC)

Sinónimos:

Rink amide linker

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About This Item

Fórmula empírica (notación de Hill):
C32H29NO7
Número de CAS:
145069-56-3
Peso molecular:
539.58
Beilstein/REAXYS Number:
5841553
MDL number:
MFCD00153509
UNSPSC Code:
12352200
PubChem Substance ID:
57649865
NACRES:
NA.22

assay

≥99.0% (HPLC)

form

solid

reaction suitability

reagent type: cross-linking reagent

mp

~180 °C (dec.)

functional group

Fmoc
amine
carboxylic acid

storage temp.

2-8°C

SMILES string

O=C(O)COC1=CC=C(C=C1)C(NC(OCC2C(C=CC=C3)=C3C4=C2C=CC=C4)=O)C5=CC=C(OC)C=C5OC

InChI

1S/C32H29NO7/c1-37-22-15-16-27(29(17-22)38-2)31(20-11-13-21(14-12-20)39-19-30(34)35)33-32(36)40-18-28-25-9-5-3-7-23(25)24-8-4-6-10-26(24)28/h3-17,28,31H,18-19H2,1-2H3,(H,33,36)(H,34,35)

InChI key

UPMGJEMWPQOACJ-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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Certificados de análisis (COA)

Lot/Batch Number
BCCC0733
BCBJ9481V
1346336V
1346336
1333514

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Hiroshi Hinou et al.
Bioorganic & medicinal chemistry, 27(13), 2822-2831 (2019-05-14)
Structural and functional effects of core M1 type glycan modification catalyzed by protein O-linked mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGnT1) were investigated using a core M1 glycoform focused library of an α-dystroglycan fragment, 372TRGAIIQTPTLGPIQPTRV390. Evanescent-field fluorescence-assisted microarray system illuminated the specific binding
Thomas H Craven et al.
Scientific reports, 8(1), 13490-13490 (2018-09-12)
Serine proteases are released by neutrophils to act primarily as antimicrobial proteins but excessive and unbalanced serine protease activity results in serious host tissue damage. Here the synthesis of a novel chemical sensor based on a multi-branched fluorescence quencher is
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Journal of materials science. Materials in medicine, 29(5), 62-62 (2018-05-08)
The present work is focused on the design of a bioactive chitosan-based scaffold functionalized with organic and inorganic signals to provide the biochemical cues for promoting stem cell osteogenic commitment. The first approach is based on the use of a
Lubinda Mbundi et al.
Nanomaterials (Basel, Switzerland), 8(6) (2018-06-06)
The control of osteoblast/osteoclast cross-talk is crucial in the bone remodelling process and provides a target mechanism in the development of drugs for bone metabolic diseases. Osteoprotegerin is a key molecule in this biosignalling pathway as it inhibits osteoclastogenesis and

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