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Merck
CN

N1909

1-萘甲酸

96%

别名:

1-萘酸

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关于此项目

线性分子式:
C10H7CO2H
化学文摘社编号:
分子量:
172.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-681-9
Beilstein/REAXYS Number:
1908896
MDL number:
Assay:
96%
Form:
powder
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InChI

1S/C11H8O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,(H,12,13)

InChI key

LNETULKMXZVUST-UHFFFAOYSA-N

SMILES string

OC(=O)c1cccc2ccccc12

assay

96%

form

powder

bp

300 °C (lit.)

mp

157-160 °C (lit.)

Quality Level

Application

1-萘甲酸可作为以下应用的反应剂:
  • 在铑催化剂存在下,与炔烃通过脱水环化反应制备萘嵌苯酮。
  • 使用Rh催化剂,与2-丁炔通过有氧的氧化环化反应制备异香豆素衍生物。
  • N,O-二甲基羟胺和三氯化磷反应制备N-甲氧基-N-甲基-1-萘甲酰胺(Weinreb酰胺)。
  • 通过Birch还原反应制备1,4-二氢-1-萘羧酸。

Other Notes

残留物为 2-萘甲酸

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yu-mei Song et al.
Chemical communications (Cambridge, England), 48(7), 1006-1008 (2011-12-14)
Reversible single-crystal-to-single-crystal transformation (SCSC) was for the first time observed between 4f-based molecular magnets.
S Chandra et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(3), 704-713 (2009-09-02)
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
Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate.
Da-Gang Yu et al.
Angewandte Chemie (International ed. in English), 50(31), 7097-7100 (2011-06-29)
Qunfei Zhao et al.
Chemistry & biology, 15(7), 693-705 (2008-07-19)
Azinomycin B is a complex natural product containing densely assembled functionalities with potent antitumor activity. Cloning and sequence analysis of the azi gene cluster revealed an iterative type I polyketide synthase (PKS) gene, five nonribosomal peptide synthetases (NRPSs) genes and
Rajesh Sunasee et al.
The Journal of organic chemistry, 73(20), 8016-8020 (2008-09-26)
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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