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Merck

N4002

Sigma-Aldrich

2-萘乙酸

99%

别名:

2-萘基乙酸

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About This Item

线性分子式:
C10H7CH2CO2H
CAS号:
分子量:
186.21
Beilstein:
973396
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

99%

表单

crystals

mp

141-143 °C (lit.)

SMILES字符串

OC(=O)Cc1ccc2ccccc2c1

InChI

1S/C12H10O2/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H,13,14)

InChI key

VIBOGIYPPWLDTI-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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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E Abuin et al.
Journal of colloid and interface science, 283(1), 87-93 (2005-02-08)
A study has been made of the effect of urea upon the hydrolysis of 2-naphthyl acetate (2-NA) catalyzed by lipase from Rhizopus arrhizus in AOT-heptane-water reverse micellar solutions at pH 7. The partition constants, K, of 2-NA between n-heptane and
Hiroshi Ikeda et al.
Organic letters, 5(10), 1625-1627 (2003-05-09)
[reaction: see text] 6(A),6(D)-Bispyridinio-appended gamma-cyclodextrin effectively enhanced the excimer fluorescence of 2-naphthylacetate. This increase derived from the increase of formation of the 1:2 complex between the cation-charged gamma-cyclodextrin and 2-naphthylacetate by the electrostatic interaction between the host and the guest.
M V Marsh et al.
Xenobiotica; the fate of foreign compounds in biological systems, 11(10), 655-663 (1981-10-01)
1. 14C-Labelled benzoic acid, salicylic acid and 2-naphthylacetic acid were administered orally to horses, and urinary metabolites investigated by chromatographic and mass spectral techniques. 2. [14C]Benzoic acid (5 mg/kg) was eliminated rapidly in the urine, and quantitatively recovered in 24
V Simeon et al.
Chemico-biological interactions, 87(1-3), 103-107 (1993-06-01)
The heat inactivation of esterases in human and rabbit serum was followed at 50 and 55 degrees C by measuring the decrease of activity with paraoxon, phenylacetate and beta-naphthylacetate as substrates. The rate of inactivation measured with the three substrates
T S Emudianughe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 17(7), 815-821 (1987-07-01)
The patterns of metabolic conjugation of the isomeric 1- and 2-naphthylacetic acids have been compared in guinea pig, mouse, hamster and gerbil. Equimolar doses of [carboxy-14C]1- and 2-naphthylacetic acids were given to these species by i.p. injection, their urine collected

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