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MFCD00161818 molecular structure
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ChemBase ID: 146334
Molecular Formular: C24H23O4
Molecular Mass: 375.43702
Monoisotopic Mass: 375.15963422
SMILES and InChIs

SMILES:
*/C=C/c1ccc(cc1)COc1ccc(cc1)C(c1ccc(cc1OC)OC)O
Canonical SMILES:
*/C=C/c1ccc(cc1)COc1ccc(cc1)C(c1ccc(cc1OC)OC)O
InChI:
InChI=
InChIKey:

Cite this record

CBID:146334 http://www.chembase.cn/molecule-146334.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
Synonyms
(4-[(2,4-Dimethoxyphenyl)hydroxymethyl]phenol, polymer-bound
Rink acid-labile (hydroxymethyl)polystyrene
Rink acid resin
Rink 酸不稳定(羟甲基)聚苯乙烯
聚合物键合型 (4-[(2,4-二甲氧基苯基)羟甲基]苯酚
Rink 酸树脂
MDL Number
MFCD00161818
PubChem SID
24873895
24878043
162240532
PubChem CID
4142055

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 4142055 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
36/37/38 expand Show data source
Safety Statements
26-36 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H315-H319-H335 expand Show data source
GHS Precautionary statements
P261-P305 + P351 + P338 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves expand Show data source
Particle Size
100-200 mesh expand Show data source
50-100 mesh expand Show data source
Extent of Labeling
0.5-1.5 mmol/g loading expand Show data source
0.6-0.8 mmol/g loading expand Show data source
Crosslinking
1 % cross-linked with divinylbenzene expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 516597 external link
Packaging
5 g in glass bottle
Application

• Acid labile resin used in Fmoc-based solid phase peptide synthesis (SPPS).
• Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.
• Cleavage of the final protected peptide can be achieved in as little as 10% AcOH in DCM or 1% TFA in DCM.
Sigma Aldrich - 534528 external link
Packaging
5 g in glass bottle
Application

• Acid labile resin used in Fmoc-based solid phase peptide synthesis.
• Mild acidic cleavage conditions lead to the release of the peptide acid where fully protected peptides can be released if desired.
• Cleavage of the final protected peptide can be achieved in as little as 10% AcOH in DCM or 1% TFA in DCM.

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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