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A38800

Sigma-Aldrich

2-氨基蒽

96%

别名:

2-蒽胺

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About This Item

经验公式（希尔记法）:
C14H11N
CAS号:
613-13-8
分子量:
193.24
Beilstein:
2209414
EC 号:
210-330-9
MDL编号:
MFCD00003582
UNSPSC代码:
12352100
PubChem化学物质编号:
24890821
NACRES:
NA.22

质量水平

100

方案

96%

表单

powder

mp

238-241 °C (lit.)

SMILES字符串

Nc1ccc2cc3ccccc3cc2c1

InChI

1S/C14H11N/c15-14-6-5-12-7-10-3-1-2-4-11(10)8-13(12)9-14/h1-9H,15H2

InChI key

YCSBALJAGZKWFF-UHFFFAOYSA-N

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应用

2-氨基蒽可作为反应剂用于制备：
  • 与5-α-胆甾烷-3-酮和芳香醛通过多组分环缩合反应生成类固醇衍生萘喹啉沥青质化合物。
  • 在碘催化下与芳香醛和丙酮或苯乙酮反应生成萘[2,3- f ]喹啉衍生物。

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBL1190
STBJ3963
STBG0630V
STBD3302V
STBB1901V

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Steroid-Derived Naphthoquinoline Asphaltene Model Compounds: Hydriodic Acid Is the Active Catalyst in I2-Promoted Multicomponent Cyclocondensation Reactions
Schulze M, et al.
Organic Letters, 17(23), 5930-5933 (2015)
An efficient method for the synthesis of naphthoquinoline derivatives catalyzed by iodine
Wang W, et al.
Heterocyclic Communications, 18(1), 17-21 (2012)
Rodrigo Juliano Oliveira et al.
Toxicology in vitro : an international journal published in association with BIBRA, 20(7), 1225-1233 (2006-05-24)
Due to the need to identify new antimutagenic agents and to determine their mechanism of action, the present study examined the mechanism of action of the beta-glucan with regard to antimutagenicity using the micronucleus assay in CHO-k1 and HTC cell
Katalin Jemnitz et al.
Mutagenesis, 19(3), 245-250 (2004-05-05)
We studied the replacement of hepatic S9 with in vivo and in vitro induced hepatocytes as a metabolic activation system with the aim of broadening the possibilities of mutagenic assays. Rats were pretreated with beta-naphthoflavone (BNF), phenobarbital (PB), 3-methylcholanthrene (MC)
Gemma L Ellis et al.
Journal of medicinal chemistry, 51(7), 2170-2177 (2008-03-18)
A rapid, two-step synthesis of a range of dispiro-1,2,4,5-tetraoxanes with potent antimalarial activity both in vitro and in vivo has been achieved. These 1,2,4,5-tetraoxanes have been proven to be superior to 1,2,4-trioxolanes in terms of stability and to be superior
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