Product N1909 is intended for use as a reagent in chemical synthesis rather than for use as a plant nutrient. Unfortunately, information is not available for the usage of this product for plant root development.
N1909
1-Naphthoic acid
96%
Sinonimo/i:
1-Naphthalenecarboxylic acid
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25 G
33,10 €
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Cambia visualizzazione
25 G
33,10 €
About This Item
Formula condensata:
C10H7CO2H
Numero CAS:
Peso molecolare:
172.18
Beilstein:
1908896
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
96%
Stato
powder
P. ebollizione
300 °C (lit.)
Punto di fusione
157-160 °C (lit.)
Stringa SMILE
OC(=O)c1cccc2ccccc12
InChI
1S/C11H8O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,12,13)
LNETULKMXZVUST-UHFFFAOYSA-N
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Categorie correlate
Applicazioni
1-Naphthoic acid can be used as a reactant to prepare:
- Perinaphthenones by dehydrative annulation with alkynes in the presence of rhodium catalyst.[1]
- Isocoumarin derivatives by reacting with 2-butyne via aerobic oxidative cyclization using Rh catalyst.[2]
- N-Methoxy-N-methyl-1-naphthalenecarboxamide (Weinreb amide) by reacting with N,O-dimethylhydroxylamine and phosphorus trichloride.[3]
- 1,4-Dihydro-1-naphthalenecarboxylic acid by Birch reduction.[4]
Altre note
Remainder 2-naphthoic acid
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate.
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Angewandte Chemie (International ed. in English), 50(31), 7097-7100 (2011-06-29)
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The Fourier transform infrared gas phase spectrum of Naphthoic acid (NA) was recorded in the region 4000-400 cm(-1). The Fourier transform Raman spectrum and Fourier transform IR spectra of NA were recorded in solid phase. Quantum chemical calculations of energies
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A method is described for converting tert-butyl benzoates or tert-butyl 1-naphthoates into derivatives having an alkyl or substituted alkyl group in a 1,4-relationship to an alkyl, aryl, alkenyl, or alkynyl group. Key steps in the sequence are (i) addition of
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How can it be used as plant root development
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