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Merck

68853

Supelco

异喹啉

analytical standard

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About This Item

经验公式(希尔记法):
C9H7N
CAS号:
分子量:
129.16
Beilstein:
107549
EC號碼:
MDL號碼:
分類程式碼代碼:
85151701
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

化驗

≥97.5% (GC)

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.623 (lit.)

bp

242-243 °C (lit.)

mp

26-28 °C (lit.)

密度

1.099 g/mL at 25 °C (lit.)

形式

neat

儲存溫度

2-8°C

SMILES 字串

c1ccc2cnccc2c1

InChI

1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H

InChI 密鑰

AWJUIBRHMBBTKR-UHFFFAOYSA-N

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應用

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象形圖

Skull and crossbones

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 2

閃點(°F)

215.6 °F - closed cup

閃點(°C)

102 °C - closed cup


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分析证书(COA)

Lot/Batch Number

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Yusuke Ohta
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 130(7), 925-936 (2010-07-08)
A copper-catalyzed synthesis of 2-(aminomethyl)indole through domino three-component coupling-cyclization has been developed. This reaction proceeds through Mannich-type coupling of 2-ethynylanilines, aldehydes, and secondary amines, followed by hydroamination. This indole formation was applicable to the synthesis of 4-methylene-2,3,4,9-tetrahyro-1H-pyrido[3,4-b]indoles and 5,6,7,8-tetrahydrobenzo[e]indolo[2,3-c]azepines via
Fumihiko Sato et al.
Proceedings of the Japan Academy. Series B, Physical and biological sciences, 89(5), 165-182 (2013-05-15)
Plants produce a variety of secondary metabolites that possess strong physiological activities. Unfortunately, however, their production can suffer from a variety of serious problems, including low levels of productivity and heterogeneous quality, as well as difficulty in raw material supply.
Kakali Bhadra et al.
Mini reviews in medicinal chemistry, 10(13), 1235-1247 (2010-08-19)
Alkaloids are a group of natural products with unmatched chemical diversity and biological relevance forming potential quality pools in drug screening. The molecular aspects of their interaction with many cellular macromolecules like DNA, RNA and proteins are being currently investigated
Asymmetric synthesis of isoquinoline alkaloids.
Maria Chrzanowska et al.
Chemical reviews, 104(7), 3341-3370 (2004-07-15)
Beta-phenylethylamines and the isoquinoline alkaloids.
K W Bentley
Natural product reports, 18(2), 148-170 (2001-05-05)

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