| Identification | More | [Name]
3-Phenoxy-benzaldehyde | [CAS]
39515-51-0 | [Synonyms]
3-FORMYLDIPHENYL ETHER
3-PHENOXYBENZALDEHYDE
AKOS BBS-00003181
M-PHENOXY BENZALDEHYDE
3-phenoxy-benzaldehyd
Benzaldehyde,3-phenoxy-
m-(phenyloxy)benzaldehyde
m-Phenoxybenzaldehyde 3-Phenoxybenzaldehyde
3-Phenoxybenzaldehyde,97%
(1,1'-Oxybisbebzene)-3-carbaldehyde | [EINECS(EC#)]
254-487-1 | [Molecular Formula]
C13H10O2 | [MDL Number]
MFCD00003353 | [Molecular Weight]
198.22 | [MOL File]
39515-51-0.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR YELLOW TO AMBER LIQUID | [Melting point ]
13 °C
| [Boiling point ]
169-169.5 °C11 mm Hg(lit.)
| [density ]
1.147 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.595(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [Sensitive ]
Air Sensitive | [BRN ]
511662 | [InChIKey]
MRLGCTNJRREZHZ-UHFFFAOYSA-N | [CAS DataBase Reference]
39515-51-0(CAS DataBase Reference) | [EPA Substance Registry System]
39515-51-0(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R26:Very Toxic by inhalation. | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S38:In case of insufficient ventilation, wear suitable respiratory equipment .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) . | [RIDADR ]
UN2810 - class 6.1 - PG 3 - EHS - Toxic, liquids, organic, n.o.s., HI: all | [WGK Germany ]
3
| [RTECS ]
CU7560200
| [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
29124900 | [Toxicity]
LD ipr-mus: >500 mg/kg JAFCAU26,954,78 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR YELLOW TO AMBER LIQUID | [Uses]
Deltamethrin intermediate. | [Preparation]
Synthesis of 3-Phenoxybenzaldehyde: 3-phenoxybenzoic acid is generated by catalytic oxidation of 3-phenoxytoluene, followed by electrolytic reduction to obtain Phenoxybenzyl alcohol , and then selective oxidation with sodium hypochlorite to obtain 3-Phenoxybenzaldehyde. | [Production Methods]
3-Phenoxybenzaldehyde is prepared by adding, at a relatively low temperature, a mixture of a 3-phenoxybenzyl halide and a 3-phenoxybenzal halide to a mixture of hexamethylenetetramine, acetic acid and water, the amounts of the water and acid bearing certain relationships to the amount of the mixture of halides, then heating the resulting mixture to a specified temperature level and maintaining it at that level for a specified period of time.
https://patents.google.com/patent/US4229380A/en | [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. | [Safety Profile]
Moderately toxic by intraperitoneal route. When heated to decomposition it emits acrid smoke and irritating vapors. | [Degradation]
3-Phenoxybenzoic acid(3-PBA) and 3-phenoxybenzaldehyde are the most common intermediates in the degradation pathways of Type Il pyrethroids by bacteria, except the cyfluthrin degradation in Brevibacterium aureum DG-12, the beta-cyfluthrin degradation in Pseudomonas stutzeri S1, and the fenpropathrin degradation in Clostridium sp. ZP3(Chen et al.2013a; Saikia et al.2005;Zhang et al.2011b). |
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