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安全信息

125881

Sigma-Aldrich

2,5-二溴苯胺

98%

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About This Item

线性分子式:
Br2C6H3NH2
CAS号:
3638-73-1
分子量:
250.92
EC 号:
222-865-5
MDL编号:
MFCD00007636
UNSPSC代码:
12352100
PubChem化学物质编号:
24847683
NACRES:
NA.22

质量水平

200

方案

98%

表单

solid

mp

51-53 °C (lit.)

官能团

bromo

SMILES字符串

Nc1cc(Br)ccc1Br

InChI

1S/C6H5Br2N/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2

InChI key

WRTAZRGRFBCKBU-UHFFFAOYSA-N

相关类别

应用

2,5-二溴苯胺用于合成 2,4,5-三溴苯胺 。在 2-（3,4-二甲氧基苯基）-5-溴苯并噻唑的区域选择性合成中，它也用作起始试剂 。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCM3800
BCCC7919
BCCB3086
BCBQ5034V
BCBN4278V

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L W Robertson et al.
Biochemical and biophysical research communications, 92(1), 175-182 (1980-01-15)
Du Zong-Da et al.
Journal of chromatography. A, 1616, 460791-460791 (2019-12-24)
Microporous organic network (MON) is a promise class of functional materials in solid phase extraction (SPE). However, the previous MON-based SPE works are all focused on off-line mode. The inherent drawbacks of off-line SPE such as complicated operation steps and
Zong-Da Du et al.
Talanta, 206, 120179-120179 (2019-09-14)
In this work, the magnetic amino-functionalized microporous organic network composites (Fe3O4@MON-NH2) were rational designed and facile synthesized for magnetic solid phase extraction (MSPE) of endocrine disrupting chemicals (EDCs), followed by their analysis with high-performance liquid chromatography. The incorporation of amino
Catriona G Mortimer et al.
Journal of medicinal chemistry, 49(1), 179-185 (2006-01-06)
A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved
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