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Merck

B57206

Sigma-Aldrich

3-溴苯甲醛

97%

别名:

3-溴苯甲醛, 3-甲酰基-1-溴苯, 3-甲酰基苯基溴, 3-甲酰溴苯, 5-溴苯甲醛, 间溴苯甲醛, 间甲酰基苯基溴

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About This Item

线性分子式:
BrC6H4CHO
CAS号:
分子量:
185.02
Beilstein:
1634534
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

liquid

折射率

n20/D 1.593 (lit.)

bp

233-236 °C (lit.)

mp

18-21 °C (lit.)

密度

1.587 g/mL at 25 °C (lit.)

SMILES 字串

Brc1cccc(C=O)c1

InChI

1S/C7H5BrO/c8-7-3-1-2-6(4-7)5-9/h1-5H

InChI 密鑰

SUISZCALMBHJQX-UHFFFAOYSA-N

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相关类别

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

204.8 °F - closed cup

閃點(°C)

96 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Antara Garai et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(48), 12613-12622 (2018-06-09)
Metal- versus ligand-centered redox processes and the effects of substituents on the ligands on the spectroscopic properties of the metal complexes are at the heart of research on metal complexes with non-innocent ligands. This work presents three examples of chromium
J P Fernandez et al.
Journal of medicinal chemistry, 26(9), 1317-1319 (1983-09-01)
Molecular biotransformation of 2-phenylthiazolidine (1) and its m-bromo derivative (2) in the mouse is followed by autoradiographic studies and assessed by analysis of urinary metabolites. Cysteamine (4) is one of the metabolites of compounds 1 and 2. Radioprotective activity and
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Background: Engineering a single organic-molecule-based nanoparticle integrating precise diagnosis and effective therapy is of great significance for cancer treatment and future clinical applications but remains a great challenge. The goal of this study is to explore small organic molecule-based nanoparticles
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N Ia Smoliar
Gigiena i sanitariia, (2)(2), 69-69 (1990-02-01)
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Inhibition of the enzymatic activity of histone deacetylase (HDAC) is a promising therapeutic strategy for cancer treatment and several distinct small molecule histone deacetylase inhibitors (HDACi) have been reported. We have previously identified a new class of non-peptide macrocyclic HDACi

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