B3750
N-Benzoyl-L-alanine
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About This Item
Empirical Formula (Hill Notation):
C10H11NO3
CAS Number:
Molecular Weight:
193.20
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
218-601-3
MDL number:
storage temp.
−20°C
SMILES string
C[C@H](NC(=O)c1ccccc1)C(O)=O
InChI
1S/C10H11NO3/c1-7(10(13)14)11-9(12)8-5-3-2-4-6-8/h2-7H,1H3,(H,11,12)(H,13,14)/t7-/m0/s1
InChI key
UAQVHNZEONHPQG-ZETCQYMHSA-N
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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M Cecilia Lutz et al.
International journal of food microbiology, 164(2-3), 166-172 (2013-05-18)
Putative mechanisms of action associated with the biocontrol capacity of four yeast strains (Cryptoccocus albidus NPCC 1248, Pichia membranifaciens NPCC 1250, Cryptoccocus victoriae NPCC 1263 and NPCC 1259) against Penicillium expansum and Botrytis cinerea were studied by means of in
Gottfried K Schroeder et al.
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cis-3-Chloroacrylic acid dehalogenase (cis-CaaD) from Pseudomonas pavonaceae 170 and a homologue from Corynebacterium glutamicum designated Cg10062 are 34% identical in sequence (54% similar). The former catalyzes a key step in a bacterial catabolic pathway for the nematocide 1,3-dichloropropene, whereas the
Mahmoud Hajj Chehade et al.
The Journal of biological chemistry, 288(27), 20085-20092 (2013-05-28)
Coenzyme Q (ubiquinone or Q) is a redox-active lipid found in organisms ranging from bacteria to mammals in which it plays a crucial role in energy-generating processes. Q biosynthesis is a complex pathway that involves multiple proteins. In this work