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安全信息

N4002

Sigma-Aldrich

2-萘乙酸

99%

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别名:
2-萘基乙酸
线性分子式:
C10H7CH2CO2H
CAS号:
581-96-4
分子量:
186.21
Beilstein:
973396
EC 号:
209-475-0
MDL编号:
MFCD00004126
PubChem化学物质编号:
24897359
NACRES:
NA.22

质量水平

100

检测方案

99%

形式

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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相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319 - H335

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

法规信息

农药列管产品

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L F Aguilar et al.
Archives of biochemistry and biophysics, 388(2), 231-236 (2001-05-23)
A simple method useful for the joint evaluation of substrate partitioning and kinetic parameters for reactions catalyzed by enzymes entrapped in reverse micelles is proposed. The method is applied to the hydrolysis of 2-naphthyl acetate (2-NA) catalyzed by lipase in
K Huikko et al.
Rapid communications in mass spectrometry : RCM, 17(12), 1339-1343 (2003-06-18)
The feasibility of atmospheric pressure desorption/ionization on silicon mass spectrometry (AP-DIOS-MS) for drug analysis was investigated. It was observed that only compounds with relative high proton affinity are efficiently ionized under AP-DIOS conditions. The limits of detection (LODs) achieved in
T S Emudianughe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 13(3), 133-138 (1983-03-01)
Although the occurrence of the taurine conjugation mechanism for various xenobiotic acids is well established, nothing is known of the source of the taurine used for this conjugation. [14C]Taurine was administered alone and in combination with 2-naphthylacetic acid or clofibric
The current status of attempts to predict species differences in drug metabolism.
J Caldwell
Drug metabolism reviews, 12(2), 221-237 (1981-01-01)
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
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