3-Phenoxypropionic acid

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Names

[ CAS No. ]:
7170-38-9

[ Name ]:
3-Phenoxypropionic acid

[Synonym ]:
3-Phenoxypropionic acid
MFCD00002769
EINECS 230-518-4
Propanoic acid, 3-phenoxy-
3-Phenoxypropanoic acid
b-phenoxypropionic acid
3-phenoxy-propanoic acid

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
245.0±0.0 °C at 760 mmHg

[ Melting Point ]:
98-100 °C(lit.)

[ Molecular Formula ]:
C9H10O3

[ Molecular Weight ]:
166.174

[ Flash Point ]:
107.5±13.3 °C

[ Exact Mass ]:
166.062988

[ PSA ]:
46.53000

[ LogP ]:
1.63

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.533

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
C

[ Risk Phrases ]:
34

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
3261.0

[ WGK Germany ]:
3

[ Hazard Class ]:
8.0

[ HS Code ]:
2918990090

Synthetic Route

Precursor & DownStream

Precursor

  • Ethyl acrylate TOP1 supplier
  • Phenol
  • 3-Phenoxypropanenitrile
  • 3-Phenoxy-1-propanol
  • 3-Bromopropanoic acid
  • β-Propiolactone
  • Sodium benzenolate
  • 3-Chloropropionic Acid
  • Propanoic acid,3-phenoxy-, methyl ester
  • Propanoic acid,3-(4-chlorophenoxy)-

DownStream

  • Propanoic acid,3-(4-chlorophenoxy)-
  • 7-Methoxy-1-indanone
  • 3-bromochromone
  • 4-Chromanone
  • 3-phenoxypropanamide
  • 7-Hydroxy-1-indanone
  • Propanoic acid,3-phenoxy-, methyl ester
  • Acrylic acid
  • Phenol
  • 3-Phenoxy-1-propanol

Customs

[ HS Code ]: 2918990090

[ Summary ]:
2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Novel histamine H3 receptor antagonists based on the 4-[(1H-imidazol-4-yl)methyl]piperidine scaffold.

Bioorg. Med. Chem. Lett. 16 , 395, (2006)

We report the discovery of novel histamine H(3) receptor antagonists based on 4-[(1H-imidazol-4-yl)methyl]piperidine. The most potent compounds in the series (e.g., 7) result from the attachment of a ...


More Articles


Related Compounds

  • 3-phenoxypropionic acid ethyl ester
  • 3-phenoxypropionic acid ethyl ester
  • 3-Phenoxypropionic acid trimethylsilyl ester
  • (S)-2-amino-3-phenoxypropionic acid hydrochloride
  • Benzenepropanoic acid, 4-[[2-amino-6-[4-(phenylmethyl)-1-piperazinyl]-4-pyrimidinyl]oxy]-α-methyl-α-phenoxy-
  • 3-THIOPHENEBUTANOIC ACID
  • Methyl 6,8-Di-tert-butyl-2-oxo-2H-chromene-3-carboxylate
  • ethyl 6,6-dimethyl-1H,4H,5H,6H-pyrrolo[3,4-c]pyrazole-3-carboxylate
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • Tert-butyl 5-amino-8-ethynyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 5-Iodo-6-methyl-1,3-dihydroisobenzofuran