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Merck
모든 사진(1)

문서

N4002

Sigma-Aldrich

2-Naphthaleneacetic acid

99%

동의어(들):

2-Naphthylacetic acid

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About This Item

Linear Formula:
C10H7CH2CO2H
CAS Number:
Molecular Weight:
186.21
Beilstein:
973396
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

99%

형태

crystals

mp

141-143 °C (lit.)

SMILES string

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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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Misaki Nakai et al.
Inorganic chemistry, 45(7), 3048-3056 (2006-03-28)
Two new dinuclear Ru(III) complexes containing naphthalene moieties, K[Ru2(dhpta)(mu-O2CCH2-1-naph)2] (1) and K[Ru2(dhpta)(mu-O2CCH2-2-naph)2] (2) (H5dhpta = 1,3-diamino-2-hydroxypropane-N,N,N',N'-tetraacetic acid, naph-1-CH2CO2H = 1-naphthylacetic acid, naph-2-CH2CO2H = 2-naphthylacetic acid), were synthesized. Complex 2 crystallized as an orthorhombic system having a space group of Pbca
T S Emudianughe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 17(7), 823-828 (1987-07-01)
1. The influence of dose size upon the metabolic conjugation of 2-naphthylacetic acid with various amino acids and glucuronic acid has been studied in the guinea pig, mouse and hamster. 2. Guinea pigs conjugated 2-naphthylacetic acid with glycine and glucuronic
R Darío Falcone et al.
Langmuir : the ACS journal of surfaces and colloids, 20(14), 5732-5737 (2006-02-08)
The kinetics of hydrolysis of 2-naphthyl acetate (2-NA) catalyzed by alpha-chymotrypsin (alpha-CT), in reverse micellar solutions formed by glycerol (GY)-water (38% v/v) mixture/sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/n-heptane has been determined by spectroscopic measurements. To compare the efficiency of this reaction with that
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
K Palme et al.
Symposia of the Society for Experimental Biology, 44, 299-313 (1990-01-01)
To understand precisely the mechanisms by which hormones like auxins regulate plant differentiation and development, it is essential to isolate putative hormone receptors. We have purified the major auxin binding protein from maize coleoptiles to homogeneity. The protein has an

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