3-Carboxybenzaldehyde

3-Carboxybenzaldehyde Basic information
Product Name:3-Carboxybenzaldehyde
Synonyms:3-CARBOXYBENZALDEHYDE;3-FORMYLBENZOIC ACID;CHEMPACIFIC 41257;ISOPHTHALALDEHYDIC ACID;TIMTEC-BB SBB008438;RARECHEM AL BO 0010;M-FORMYLBENZOIC ACID;3-formyl-benzoicaci
CAS:619-21-6
MF:C8H6O3
MW:150.13
EINECS:210-585-6
Product Categories:Aldehydes;Building Blocks;C8;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;CARBOXYLICACID;Aromatic Aldehydes & Derivatives (substituted)
Mol File:619-21-6.mol
3-Carboxybenzaldehyde Structure
3-Carboxybenzaldehyde Chemical Properties
Melting point 173-175 °C(lit.)
Boiling point 231.65°C (rough estimate)
density 1.2645 (rough estimate)
refractive index 1.4500 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in methanol (100 mg/mL) gives a clear to slightly hazy, colorless to very faintly brown.
pka3.84(at 25℃)
form Powder
color White to light yellow
Sensitive Air Sensitive
BRN 2206413
InChIKeyUHDNUPHSDMOGCR-UHFFFAOYSA-N
CAS DataBase Reference619-21-6(CAS DataBase Reference)
EPA Substance Registry SystemBenzoic acid, 3-formyl- (619-21-6)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 3
TSCA Yes
HS Code 29183000
MSDS Information
ProviderLanguage
3-Formylbenzoic acid English
SigmaAldrich English
ACROS English
ALFA English
3-Carboxybenzaldehyde Usage And Synthesis
Chemical Propertieswhite to light yellow powder
Uses3-Formylbenzoic acid is used in the synthesis of bicyclic cis-2-azetidinone derivatives via Ugi 4-centre 3-component reaction, porphyrin capped with a steroidal superstructure bearing convergent hydroxy groups and 3-[(4-amino-1,2-dihydro-1-oxo-2-phenyl-1,2,4-triazolo[4,3-a]quinoxalin-6-yl)amino]methyl benzoic acid.
DefinitionChEBI: 3-Formylbenzoic acid is a member of benzoic acids.
Hyaluronic acid 9-Fluorenone-4-carboxylic acid Ethyl 2-(Chlorosulfonyl)acetate 3-(Trifluoromethyl)benzaldehyde 3-Carboxybenzaldehyde MELLITIC ACID 5-Hydroxyisophthalic acid 5-Aminoisophthalic acid Folic acid 4-Hydroxybenzaldehyde 9-Fluorenone-2-carboxylic acid Benzaldehyde p-Anisaldehyde 4-Formylbenzoic acid 2-Nitrobenzaldehyde Pyromellitic acid 3-Methoxybenzaldehyde Citric acid

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