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Home > Encyclopedia > 2-(4-Bromophenoxy)acetic acid

2-(4-Bromophenoxy)acetic acid

2-(4-Bromophenoxy)acetic acid structure

2-(4-Bromophenoxy)acetic acid 

structure
  • CAS No:

    1878-91-7

  • Formula:

    C8H7BrO3

  • Chemical Name:

    2-(4-Bromophenoxy)acetic acid

  • Synonyms:

    Acetic acid,2-(4-bromophenoxy)-;Acetic acid,(p-bromophenoxy)-;Acetic acid,(4-bromophenoxy)-;2-(4-Bromophenoxy)acetic acid;(4-Bromophenoxy)acetic acid;p-Bromophenoxyacetic acid;NSC 65085

  • Categories:

    Agrochemicals  >  Plant Growth Regulators

Description

White or cream crystalline powder

2-(4-Bromophenoxy)acetic acid Basic Attributes

231.04

231.04

217-530-5

65085

DTXSID2062034

29189900

Characteristics

46.5

2.4

white crystalline powder

1.6494 (rough estimate)

160-161 °C

337.9±17.0 °C(Predicted)

158.2±20.9 °C

1.4730 (estimate)

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

3.96E-05mmHg at 25°C

Safety Information

IRRITANT

NONH for all modes of transport

3

24/25

Xi

Stable at room temperature in closed containers under normal storage and handling conditions.

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

bromophenoxyacetic acid

2-(4-Bromophenoxy)acetic acid Use and Manufacturing

Methods of Manufacturing

General procedure: A mixture of NaOH (0.04 mol, 1.60 g), deionized water (20 mL) and ethanol (20 mL) were poured into a 150 mL three-necked flask, then phenol (0.04 mol, 3.76 g) was slowly added under stirring. General procedure: Compounds B1−7 were prepared by similar procedures. In atypical synthesis of B1, monochloroacetic acid (0.04 mol, 3.78 g) was dissolved in deionized water (15 mL) under thecondition of stirring and an ice bath. Then NaOH (25 percent) wasadded dropwise until the pH value was adjusted to 9−10, thena solution of sodium chloroacetate was obtained. To a solutionof NaOH (0.03 mol, 1.20 g), deionized water (15 mL) andethanol (5 mL), phenol (0.04 mol, 3.76 g) was slowly addedunder stirring. After addition, the mixture was stirred for20 min, then the above sodium chloroacetate was addeddropwise, and heated to 105 °C and refluxed for 5 h. Thereaction mixture was cooled to room temperature. The pHvalue of the mixture was acidified to 1−2 with diluted hydrochloricacid. The precipitate was filtered, washed with dilutedhydrochloric acid many times, and recrystallized and dried invacuum, resulting in a white solid product of thephenoxyacetic acid (B1)To a stirred solution of CX (7 g, 27.02 mmol) in THF:HGeneral procedure: 55mmol monochloroacetic acid was dissolved in 15mL deionized water under the condition of ice water bath, then 30percent NaOH solution was used to adjust pH 8–9, sodium chloroacetate solution was obtained. 45mmol NaOH was dissolved in mixed solvent of 15mL deionized water and 5mL ethanol at room temperature with constant stirring, 45mmol phenol was subsequent slowly added. After stirring for another 20min, sodium chloroacetate solution was added. Subsequently, the mixture was refluxed at 102°C for 5h. After the mixture was cooled to room temperature, pH was adjusted to 1–2 with 2.0mol·L

Uses

Used as plant growth regulator

Acetic acid, 2-(4-bromophenoxy)-: INACTIVE

Computed Properties

Molecular Weight:231.04
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:229.95786
Monoisotopic Mass:229.95786
Topological Polar Surface Area:46.5
Heavy Atom Count:12
Complexity:152
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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