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138423-98-0 (3-Formyl-indol-1-yl)-acetic acid N-Acetic acid-indole-3-carboxaldehyde
Product Name: N-Acetic acid-indole-3-carboxaldehyde
Synonyms: 2-(3-methanoylindol-1-yl)ethanoic acid;3-FORMYLINDOLE-1-ACETIC ACID;(3-Formyl-1-indolyl)acetic acid≥ 97% (HPLC);1-(Carboxymethyl)indole-3-carboxaldehyde;TIMTEC-BB SBB010076;N-ACETIC ACID-INDOLE-3-CARBOXALDEHYDE;(3-FORMYL-1-INDOLYL)ACETIC ACID;3-FORMYL INDOLEACETIC ACID
CAS: 138423-98-0
MF: C11H9NO3
MW: 203.19
EINECS:
Product Categories: Indoles and derivatives;Aromatic Aldehydes & Derivatives (substituted);Heterocyclic Compounds;Indoles;Bifunctional CrosslinkersBuilding Blocks;Heterocyclic Building Blocks;Linkers;Peptide Synthesis
Mol File: 138423-98-0.mol
N-Acetic acid-indole-3-carboxaldehyde Structure
N-Acetic acid-indole-3-carboxaldehyde Chemical Properties
Melting point 197-200 °C(lit.)
Boiling point 458.5±25.0 °C(Predicted)
density 1.30±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka 4.15±0.10(Predicted)
Sensitive Air Sensitive
BRN 5431204
CAS DataBase Reference 138423-98-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
F 8-10-23
HazardClass IRRITANT
HS Code 29339900
MSDS Information
Provider Language
SigmaAldrich English
N-Acetic acid-indole-3-carboxaldehyde Usage And Synthesis
Chemical Properties Solid
Uses Handle to synthesize an indolecarboxaldehyde resin by coupling to an amino-resin. Amines and derivatives can be immobilized by reductive amination of this aldehyde resin. Mild cleavage with 50% TFA
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