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191752

Sigma-Aldrich

3-Phenoxybenzaldehyde

98%

Synonym(s):

3-Phenoxybenzaldehyde, 5-Phenoxybenzaldehyde, m-(Phenyloxy)benzaldehyde, m-Phenoxybenzaldehyde

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About This Item

Linear Formula:
C6H5OC6H4CHO
CAS Number:
39515-51-0
Molecular Weight:
198.22
Beilstein:
511662
EC Number:
254-487-1
MDL number:
MFCD00003353
UNSPSC Code:
12352100
PubChem Substance ID:
24851508
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.595 (lit.)

bp

169-169.5 °C/11 mmHg (lit.)

density

1.147 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)c1cccc(Oc2ccccc2)c1

InChI

1S/C13H10O2/c14-10-11-5-4-8-13(9-11)15-12-6-2-1-3-7-12/h1-10H

InChI key

MRLGCTNJRREZHZ-UHFFFAOYSA-N

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General description

Enantioselective autoinduction during asymmetric hydrocyanation of 3-phenoxybenzaldehyde catalyzed by cyclo[(R)-phenylalanyl-(R)-histidyl] has been investigated. It undergoes hydrogenation catalyzed by Au/Pt bimetallic core/shell nanoparticles to yield 3-phenoxyphenyl methanol.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup - (External MSDS)

Flash Point(C)

113 °C - closed cup - (External MSDS)

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sh T Iskandarova
Gigiena i sanitariia, (3)(3), 6-8 (1996-05-01)
The probable odour threshold of 3-phenoxybenzaldehyde (3-PBA) in the ambient air was estimated at 0.225 mg/m3. The maximum permissible concentration (MPC) of 3-PBA on a single exposure was recommended to be 0.09 mg/m3. The mean daily MPC of 3-PBA was
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The application of unusual high pH-values within enzymatic cyanohydrin synthesis has been investigated. Usually enzymatic cyanohydrin synthesis in two-phase systems requires low pH-values within the aqueous phase to suppress the non-enzymatic side reaction. In contrast, we investigated the usage of
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Archives of insect biochemistry and physiology, 69(1), 13-21 (2008-07-11)
Metabolism by cytochrome P450 monooxygenases is a major mechanism implicated in resistance of insects to insecticides, including pyrethroids. We previously isolated the cytochrome P450 CYP6AA3 from deltamethrin-selected resistant strain of Anopheles minimus mosquito, a major malaria vector in Thailand. In
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