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405426

Sigma-Aldrich

2,6-双(溴甲基)吡啶

98%

别名:

α,α′-二溴-2,6-二甲基吡啶, 1,6-二溴甲基吡啶, 2,6-二溴甲基吡啶

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About This Item

经验公式（希尔记法）:
C7H7Br2N
CAS号:
7703-74-4
分子量:
264.95
MDL號碼:
MFCD00191795
分類程式碼代碼:
12352100
PubChem物質ID:
24865316
NACRES:
NA.22

一般說明

2,6-二（溴甲基）吡啶晶体具有通过 c 滑移面作用相关的分子。分子沿 c 轴排列成堆。其参与双阳离子咪唑连接环番的合成。

應用

2,6-双（溴甲基）吡啶可用于制备以下物质：
  • 一种新的吡啶-吡唑衍生物，2,6-双（3,5-二苯吡唑-1-基甲基）吡啶
  • 一个大的大环配体，N(1),N(7)-吡啶-2,6-二甲基-N(2),N(6)-双（(6-(3-(1H苯并[d] 咪唑-1-基）丙酰胺基）吡啶-2-基）吡啶-2,6-二甲酰胺二溴
  • 小环、潜在三齿 Se (2) N （吡啶基）-供体大环

象形圖

Exclamation mark
GHS07

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

11 - Combustible Solids

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

dust mask type N95 (US), Eyeshields, Gloves

从最新的版本中选择一种：

分析证书(COA)

Lot/Batch Number
MKCM2538
MKCC7245
MKBS3382V
MKBK5803V
MKBF8986V

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William Levason et al.
Dalton transactions (Cambridge, England : 2003), (23)(23), 4569-4577 (2009-06-03)
Simultaneous dropwise addition of thf/EtOH solutions of Se{(CH(2))(3)OTs}(2) and o-C(6)H(4)(CH(2)SeCN)(2) or NCSe(CH(2))(3)SeCN to a suspension of NaBH(4) in thf/EtOH at room temperature yields gram quantities of the 13- and 12-membered triselenoether macrocycles (1) and (2) respectively in high yield. The
Hanna S Abbo et al.
Molecules (Basel, Switzerland), 18(4), 4728-4738 (2013-04-24)
The tridentate ligand 2,6-bis(3,5-diphenylpyrazol-1-ylmethyl)pyridine, abbreviated as 2,6-[(3,5-ph₂pz-CH₂)₂-py], a new pyridine-pyrazole derivative, was prepared from 2,6-bis(bromomethyl)pyridine and 3,5-diphenylpyrazole. The ligand was characterized by means of elemental analyses, ATR-IR, ¹H- and ¹³C-NMR spectroscopy and single crystal X-ray crystallography. Using this ligand, a
Kim Meyer et al.
Dalton transactions (Cambridge, England : 2003), 41(46), 14059-14067 (2012-09-11)
Treatment of N(2),N(6)-bis(6-acrylamidopyridin-2-yl)pyridine-2,6-dicarboxamide with benzimidazole gives the acyclic aza-Michael addition product N(2),N(6)-bis(6-(3-(1H-benzo[d]imidazol-1-yl)propanamido)pyridin-2-yl)pyridine-2,6-dicarboxamide (2). The macrocycle N(1),N(7)-pyridine-2,6-dimethyl-N(2),N(6)-bis(6-(3-(1H-benzo[d]imidazol-1-yl)propanamido)pyridin-2-yl)pyridine-2,6-dicarboxamide dibromide ([H(2)L(2)]Br(2)) is formed through the double alkylation of 2 with 2,6-bis(bromomethyl)pyridine. The imidazole analogues of 2 and [H(2)L(2)]Br(2) (1 and [H(2)L(1)]Br(2), respectively) have
Synthesis of an imidazolium-linked cyclophane from histamine.
Durmus S, et al.
Tetrahedron, 61(1), 97-101 (2005)
2, 6-Bis(bromomethyl) pyridine.
Cuzan O, et al.
Acta Crystallographica Section E, Structure Reports Online, 70(1), 4-4 (2014)

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