1-NAPHTHHYDRAZIDE

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Products Intro: Product Name:1-Naphthhydrazide
CAS:43038-45-5
Purity:0.98 Package:1g;5g;25g;100;500g
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Products Intro: CAS:43038-45-5
Purity:0.99 Package:1kg
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Products Intro: Product Name:1-NAPHTHHYDRAZIDE
CAS:43038-45-5
Purity:99% Package:1KG;9.20USD
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Products Intro: Product Name:1-NAPHTHHYDRAZIDE
CAS:43038-45-5
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Products Intro: Product Name:1-Naphthoic hydrazide
CAS:43038-45-5
Purity:0.95&0.99 Package:0.1KG;1KG;1000KG Remarks:Factory Supply
1-NAPHTHHYDRAZIDE Basic information
Product Name:1-NAPHTHHYDRAZIDE
Synonyms:ALPHA-NAPHTHOYLHYDRAZINE;AKOS BC-1515;1-NAPHTHOIC HYDRAZIDE;1-NAPHTHOIC ACID HYDRAZIDE;1-NAPHTHHYDRAZIDE;1-NAPHTHALENECARBOHYDRAZIDE;1-Naphthalenecarboxylic acid, hydrazide;1-Naphthoylhydrazine
CAS:43038-45-5
MF:C11H10N2O
MW:186.21
EINECS:256-054-2
Product Categories:Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes;Miscellaneous Compounds
Mol File:43038-45-5.mol
1-NAPHTHHYDRAZIDE Structure
1-NAPHTHHYDRAZIDE Chemical Properties
Melting point 166-168°C
density 1.232±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka12.65±0.30(Predicted)
color White to Light yellow
BRN 2966714
InChIInChI=1S/C11H10N2O/c12-13-11(14)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,12H2,(H,13,14)
InChIKeyVMFUMDXVTKTZQY-UHFFFAOYSA-N
SMILESC1(C(NN)=O)=C2C(C=CC=C2)=CC=C1
CAS DataBase Reference43038-45-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
HS Code 2928.00.2500
HazardClass IRRITANT
MSDS Information
ProviderLanguage
ALFA English
1-NAPHTHHYDRAZIDE Usage And Synthesis
Synthesis
1-NAPHTHOIC ACID METHYL ESTER

2459-24-7

1-NAPHTHHYDRAZIDE

43038-45-5

General procedure for the synthesis of 1-naphthylhydrazine from methyl 1-naphthalenecarboxylate: Methyl 1-naphthalenecarboxylate (0.52 g, 2.8 mmol) was dissolved in 15 mL of 98% hydrazine hydrate, fitted with an air condenser tube, and the reaction was stirred for 8 h at 110 °C. The reaction was carried out in the presence of an air condenser tube. Upon completion of the reaction, the mixture was cooled to room temperature and the precipitated crystalline solid was collected by filtration. The resulting solid was dissolved in ethyl acetate (EtOAc), and the organic phase was washed sequentially with water, saturated sodium bicarbonate (NaHCO3) solution and brine, and then concentrated under reduced pressure to remove the solvent. The product was purified by column chromatography (elution gradient: hexane/ethyl acetate 1:1; hexane/ethyl acetate 1:2) to give 0.38 g (73% yield) of white crystalline solid. Thin layer chromatography (TLC) Rf = 0.53 (unfolding agent: chloroform/methanol 10:1). Melting point 166-169 °C (literature value 166 °C).IR (KBr, cm-1): νmax 3280 (N-H), 1658 (C=O), 1606, 1588, 1524, 1261, 955.1H NMR (300 MHz, DMSO-d6): δ 9.69 (s, 1H, NH), 8.35-8.10 (m. 1H, Ar-H), 8.05-7.88 (m, 2H, Ar-H), 7.63-7.26 (m, 4H, Ar-H), 4.60 (s, 2H, NH2).13C NMR (75 MHz, DMSO-d6): δ 168.2 (C=O), 133.6, 133.3, 130.2, 130.1, 128.4, 128.4 126.8, 126.4, 125.6, 125.6, 125.2 (Ar-C).

References[1] European Journal of Medicinal Chemistry, 2016, vol. 120, p. 97 - 110
[2] Journal of the American Chemical Society, 2010, vol. 132, # 20, p. 6900 - 6901
[3] Chemistry - A European Journal, 2011, vol. 17, # 30, p. 8294 - 8298
[4] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 11, p. 3615 - 3621
[5] RSC Advances, 2015, vol. 5, # 37, p. 28996 - 29001
1-NAPHTHHYDRAZIDE Preparation Products And Raw materials
Raw materials1-NAPHTHOIC ACID METHYL ESTER-->1-Naphthoyl chloride-->ETHYL 1-NAPHTHOATE-->1-Bromonaphthalene-->1-Naphthoic acid
Preparation Products5-(naphthalen-1-yl)-1,3,4-oxadiazole-2-thiol
Tag:1-NAPHTHHYDRAZIDE(43038-45-5) Related Product Information
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