565040
3-Chloro-4-methoxybenzaldehyde
97%
Synonym(s):
3-Chloro-p-anisaldehyde
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About This Item
Linear Formula:
CH3OC6H3ClCHO
CAS Number:
Molecular Weight:
170.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
56-60 °C (lit.)
SMILES string
[H]C(=O)c1ccc(OC)c(Cl)c1
InChI
1S/C8H7ClO2/c1-11-8-3-2-6(5-10)4-7(8)9/h2-5H,1H3
InChI key
WYVGYYIZXPXHAZ-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Dongfei Han et al.
PloS one, 8(9), e73350-e73350 (2013-09-26)
A novel flavoprotein monooxygenase, trans-anethole oxygenase (TAO), from Pseudomonas putida JYR-1, which is capable of catalyzing the oxidation of trans-anethole to p-anisaldehyde, was heterologously expressed in E. coli and purified. Enzymatic kinetics of diverse substrates and cofactors revealed that TAO
E de Jong et al.
FEBS letters, 305(3), 220-224 (1992-07-06)
The white-rot fungus Bjerkandera sp. BOS55 produced de-novo several aromatic metabolites. Besides veratryl alcohol and veratraldehyde, compounds which are known to be involved in the ligninolytic system of several other white-rot fungi, other metabolites were formed. These included anisaldehyde, 3-chloro-anisaldehyde
T Mester et al.
Applied and environmental microbiology, 63(5), 1987-1994 (1997-05-01)
Aryl metabolites are known to have an important role in the ligninolytic system of white rot fungi. The addition of known precursors and aromatic acids representing lignin degradation products stimulated the production of aryl metabolites (veratryl alcohol, veratraldehyde, p-anisaldehyde, and
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