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Merck

407518

Sigma-Aldrich

久洛利定 氢溴酸盐

97%

别名:

2,3,6,7-四氢-1H,5H-苯并[ij]喹嗪 氢溴酸盐

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About This Item

经验公式(希尔记法):
C12H15N · HBr
CAS号:
分子量:
254.17
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

powder

mp

239-242 °C (lit.)

SMILES 字串

Br.C1CN2CCCc3cccc(C1)c23

InChI

1S/C12H15N.BrH/c1-4-10-6-2-8-13-9-3-7-11(5-1)12(10)13;/h1,4-5H,2-3,6-9H2;1H

InChI 密鑰

KHWBRFVBPGPEOJ-UHFFFAOYSA-N

一般說明

Julolidines are effective auxofluors that are employed in laser dyes and biochemical stains. They are known to be one of the strongest electron-releasing groups due to electronic and steric factors.

應用

Julolidine hydrobromide may be used in the synthesis of [4-(2,3,6,7-tetrahydro-1H,5H-pyrido[3,2,1-ij]quinolin-9-ylazo)-phenyl]-methanol azodye.

象形圖

CorrosionSkull and crossbones

訊號詞

Danger

危險分類

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B

安全危害

儲存類別代碼

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


分析证书(COA)

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Synthesis, optical characterization and crystal and molecular X-ray structure of a phenylazojulolidine derivative.
Barbero N, et al.
Dyes and Pigments, 92(3), 1177-1183 (2012)
Synthesis of julolidine derivatives.
Kauffman JM, et al.
Organic preparations and procedures international, 33(6), 603-613 (2001)

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