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1,2-Phenylenediacetic acid

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1,2-Phenylenediacetic acid Basic information

Product Name:
1,2-Phenylenediacetic acid
Synonyms:
  • BENZENE-1,2-DIACETIC ACID
  • 1,2-PHENYLENEDIACETIC ACID
  • 2-Phenylenediacetic acid
  • o-Phenylenediacetic acid, 98+%
  • RARECHEM AL BO 0119
  • O-PHENYLENEDIACETIC ACID
  • O-BENZENEDIACETIC ACID
  • 1,2-Benzenediacetic acid
CAS:
7500-53-0
MF:
C10H10O4
MW:
194.18
EINECS:
231-355-1
Product Categories:
  • Aromatic Phenylacetic Acids and Derivatives
  • C10
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
7500-53-0.mol
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1,2-Phenylenediacetic acid Chemical Properties

Melting point:
150-152 °C (lit.)
Boiling point:
290.62°C (rough estimate)
Density 
1.2534 (rough estimate)
refractive index 
1.5430 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
Needle-Like Crystalline Powder
pka
3.90±0.10(Predicted)
color 
Beige to beige-brown
BRN 
2616747
InChI
InChI=1S/C10H10O4/c11-9(12)5-7-3-1-2-4-8(7)6-10(13)14/h1-4H,5-6H2,(H,11,12)(H,13,14)
InChIKey
MMEDJBFVJUFIDD-UHFFFAOYSA-N
SMILES
C1(CC(O)=O)=CC=CC=C1CC(O)=O
CAS DataBase Reference
7500-53-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29173990

MSDS

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1,2-Phenylenediacetic acid Usage And Synthesis

Chemical Properties

beige to beige-brown needle-like crystalline

Uses

1,2-Phenylenediacetic Acid has been used in the preparation of nanomolar inhibitors of cancer-relevant transcription factor STAT5b.

General Description

A coordination polymer with 1,2-Phenylenediacetic acid was synthesized and characterized by single crystal X-ray diffraction.

Synthesis

613-73-0

7500-53-0

The general procedure for the synthesis of 2,2'-(1,2-phenylene)diacetic acid from 1,2-phenylenediacetonitrile was as follows: 1,2-phenylenediacetonitrile (5.0 g) was dissolved in 50 mL of concentrated hydrochloric acid and heated and refluxed for 3 hours. After the reaction was completed, 30 mL of water was added and heating was continued overnight. The reaction mixture was cooled to room temperature and washed with ether. Subsequently, the organic layer was extracted twice with aqueous sodium carbonate. The aqueous layers were combined, acidified to pH 2-3 with hydrochloric acid and extracted with ether. The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated to give 2,2'-(1,2-phenylene)diacetic acid as a light yellow solid in 56% yield with a melting point of 123-125 °C. The product was confirmed by 1H NMR (250 MHz, DMSO-d6): δ 3.58 (s, 4H), 7.20 (s, 4H), 12.34 (br s, 2H); 13C NMR (63 MHz, DMSO-d6): δ 37.1 (2C), 126.8 (2C), 130.6 (2C), 134.1 (2C), 172.4 (2C).

References

[1] Patent: WO2011/41349, 2011, A1. Location in patent: Page/Page column 19-20
[2] Chemische Berichte, 1884, vol. 17, p. 447
[3] Journal of the Chemical Society, 1907, vol. 91, p. 176
[4] Journal of the Chemical Society, 1923, vol. 123, p. 2075
[5] Recueil des Travaux Chimiques des Pays-Bas, 1923, vol. 42, p. 412

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