648744
Mandelamide
97%
Synonym(s):
2-Hydroxy-2-phenylacetamide
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About This Item
Linear Formula:
C6H5CH(OH)CONH2
CAS Number:
Molecular Weight:
151.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
133-137 °C (lit.)
SMILES string
NC(=O)C(O)c1ccccc1
InChI
1S/C8H9NO2/c9-8(11)7(10)6-4-2-1-3-5-6/h1-5,7,10H,(H2,9,11)
InChI key
MAGPZHKLEZXLNU-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
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
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Clemens Lamberth et al.
Pest management science, 63(1), 57-62 (2006-11-02)
Novel analogues of mandipropamid have been designed and prepared. The synthetic approach to these stretched and heterocyclic mandelamides is outlined. Biological data demonstrate their high efficacy against important plant diseases like tomato and potato late blight (Phytophthora infestans De Bary)
Zi Wei Luo et al.
Metabolic engineering, 62, 298-311 (2020-10-18)
Benzoic acid (BA) is an important platform aromatic compound in chemical industry and is widely used as food preservatives in its salt forms. Yet, current manufacture of BA is dependent on petrochemical processes under harsh conditions. Here we report the
[Molecular biology aspects of the antimicrobial effect of synthetic chemotherapeutic agents].
N Popov
Zeitschrift fur arztliche Fortbildung, 76(15), 662-666 (1982-08-01)
Michael J McLeish et al.
Journal of bacteriology, 185(8), 2451-2456 (2003-04-03)
The enzymes of the mandelate metabolic pathway permit Pseudomonas putida ATCC 12633 to utilize either or both enantiomers of mandelate as the sole carbon source. The genes encoding the mandelate pathway were found to lie on a single 10.5-kb restriction
Pan-Fen Wang et al.
Protein engineering, design & selection : PEDS, 22(2), 103-110 (2008-12-17)
Mandelamide hydrolase (MAH), a member of the amidase signature family, catalyzes the hydrolysis of mandelamide to mandelate and ammonia. X-ray structures of several members of this family, but not that of MAH, have been reported. These reveal nearly superimposable conformations
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