2,6-二溴吡啶 | 626-05-1
中文名称:
2,6-二溴吡啶
英文名称:
2,6-Dibromopyridine
CAS No.:
626-05-1
分子式:
C5 H3 Br2 N
分子量:
236.8920
名称和标识符
MDL
MFCD00006223
InChIKey
FEYDZHNIIMENOB-UHFFFAOYSA-N
Inchi
1S/C5H3Br2N/c6-4-2-1-3-5(7)8-4/h1-3H
SMILES
BrC1C([H])=C([H])C([H])=C(N=1)Br
BRN
0108922
别名信息
- 中文别名 -
2,6-二溴吡啶
2 . 6 - 二 溴 吡 啶
2,6-Dibromopyridine 2,6-二溴吡啶
二溴呲啶
- 英文别名 -
2,6-Dibromopyridine
2,5-Dibromopyridine
2.6-Dibromopyridine
1,5-dibromopyridine
1,6-dibromopyridine
2,6-dibromolutidene
2,6-dibromo-pyridin
2,6-dibromo-pyridine
2,6-DibroMopyridine 25GR
Pyridine,2,6-dibromo
PYRIDINE, 2,6-DIBROMO-
2,6-dibromo pyridine
FEYDZHNIIMENOB-UHFFFAOYSA-N
NSC613
2,6dibromopyridine
2,6-dibrompyridine
2,6 dibromopyridine
PubChem3204
2, 6-Dibromopyridine
KSC353O0L
ARONIS25134
STR02550
BCP22162
SBB059469
RM0220
RW201
2,6-dibromopyridine
A937236
EINECS 210-926-9
GEO-00971
D9SBA5R353
FT-0610561
AB00637
MFCD00006223
FG-0512
W-203332
2,6-Dibromopyridine, 98%
DTXSID30211642
NSC-613
BRN 0108922
626-05-1
AC-15880
EN300-18091
2,6-Dibromopyridine,
A8655
AKOS000119683
D1555
2.6-dibromopyridine
NS00035094
Q209274
doi:10.14272/FEYDZHNIIMENOB-UHFFFAOYSA-N.2
NSC 613
HY-59162
SCHEMBL3973
UNII-D9SBA5R353
5-20-05-00435 (Beilstein Handbook Reference)
AM81197
CS-W008833
BP-12334
F8881-3979
2,6-Dibromopyridine,97%
物化性质
实验特性
LogP
2.60660
PSA
12.89000
折射率
1.5800 (estimate)
水溶性
不溶
沸点
249°C(lit.)
熔点
117.0 to 120.0 deg-C
闪点
华氏:>212 °F 摄氏:>100 °C
颜色与性状
微白色粉末。
溶解性
不溶于水。
敏感性
对光敏感
密度
2.0383 (rough estimate)
计算特性
精确分子量
234.86300
氢键供体数量
0
氢键受体数量
1
可旋转化学键数量
0
同位素质量
234.863
重原子数量
8
复杂度
68.8
同位素原子数量
0
确定原子立构中心数量
0
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
2.9
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
12.9
海关数据
海关编码
29333999
海关数据
中国海关编码:
2933399090
概述:
2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素:
品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
相关文献
1.
Selective palladium-catalysed arylation of 2,6-dibromopyridine using N-heterocyclic carbene ligands
D. Prajapati,C. Schulzke,M. K. Kindermann,A. R. Kapdi RSC Adv. 2015 5 53073
2.
Direct access to 2-(hetero)arylated pyridines from 6-substituted 2-bromopyridines via phosphine-free palladium-catalyzed C–H bond arylations: the importance of the C6 substituent
Wided Hagui,Néji Besbes,Ezzeddine Srasra,Jean-Fran?ois Soulé,Henri Doucet RSC Adv. 2016 6 17110
3.
10 gram-scale synthesis of a chiral oxazoline iminopyridine ligand and its applications
Jianhui Chen,Tuo Xi,Zhan Lu Org. Chem. Front. 2018 5 247
4.
Novel diphenylphosphine derivatives of 2,2′-bithiophene, 2,2′:5′,2″-terthiophene, 2-(2′-thienyl)pyridine and 2,6-di-2′-thienylpyridine. Crystal structures of 5,5′-bis(diphenylphosphino)-2,2′-bithiophene, diphenyl{5-[6′-(diphenylphosphino)-2′-pyridyl]-2-thienyl}phosphine and 2,6-bis[5′-(diphenylphosphino)-2′-thienyl]pyridine
John S. Field,Raymond J. Haines,Elena I. Lakoba,M. Hal Sosabowski J. Chem. Soc. Perkin Trans. 1 2001 3352
5.
Synthesis and electronic investigation of mono- and di-substituted 4-nitro- and 4-amino-pyrazol-1-yl bis(pyrazol-1-yl)pyridine-type ligands and luminescent Eu(iii) derivatives
D. J. Strohecker,V. M. Lynch,B. J. Holliday,R. A. Jones Dalton Trans. 2017 46 7733
6.
Ligands containing alternating 2,6-linked pyridine and 2,5-linked thiophene units?1
Otto Meth-Cohn,Hui Jiang J. Chem. Soc. Perkin Trans. 1 1998 3737
7.
Design, synthesis and excited-state properties of mononuclear Ru(ii) complexes of tridentate heterocyclic ligands
Amlan K. Pal,Garry S. Hanan Chem. Soc. Rev. 2014 43 6184
8.
Luminescent porous organic polymer nanotubes for highly selective sensing of H2S
Lin Guo,Meng Wang,Xiaofei Zeng,Dapeng Cao Mater. Chem. Front. 2017 1 2643
9.
Structural, electrochemical and photophysical behavior of Ru(ii) complexes with large bite angle sulfur-bridged terpyridyl ligands
Christopher M. Brown,Nicole E. Arsenault,Trevor N. K. Cross,Duane Hean,Zhen Xu,Michael O. Wolf Inorg. Chem. Front. 2020 7 117
10.
Facile synthesis of α-alkoxyl amides via scandium-catalyzed oxidative reaction between ynamides and alcohols
Zhi-Xin Zhang,Bo-Han Zhu,Pei-Xi Xie,Jia-Qi Tang,Xin-Ling Li,Chunyin Zhu,Ying-Wu Yin,Long-Wu Ye RSC Adv. 2018 8 18308
参考资料
Reaxys RN
108922
Beilstein
20(2)153
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上游
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2,6-二溴吡啶-4-醇
2-溴-6-碘吡啶
2,4,6-三溴吡啶
2-溴-6-哌啶基吡啶
2,6-二溴吡啶氧化物
2-氯-6-碘吡啶
2-溴-6-肼基吡啶
6-BROMO-(4-METHOXYBENZYLAMINO)PYRIDINE
4-溴-2,6-二氨基吡啶
2-溴-6-吡啶甲醇
6-溴-2-吡啶甲醛
2,2'-联吡啶
2-溴-6-苯基吡啶
2,6-di-(1-piperidinyl)pyridine
2,6-二溴-3-氨基吡啶
2-氯-6-(三氟甲基)吡啶
2-BENZYLAMINO-6-BROMOPYRIDINE
2-乙氧基-6-溴吡啶
2-溴-6-乙酰基吡啶
2-溴-6-(2-甲基-1,3-二氧戊烷-2-基)吡啶
tris[2-(6-bromopyridyl)]phosphine
6,6'-二溴-2,2'-联吡啶
2-溴-6-氯吡啶
2,6-二碘吡啶
2,6-二溴-3-甲醛
2-(6-溴吡啶-2-基)丙烷-2-醇
6-溴嘧啶-2-硼酸频哪酯
6-氯吡啶-2-硼酸频哪酯
2,6-二(乙炔基)吡啶
2-溴-alpha-甲基-3-吡啶甲醇
6-溴-2-二乙基氨基吡啶
2-Pyridinecarboxaldehyde,6-[2-(4-methylphenyl)-1,3-dioxolan-2-yl]-
阿伐斯汀
6-溴-2-甲基氨基吡啶
3-氨基-2-甲氧基-6-溴吡啶
6-溴-2-吡啶磺酰氯
与2,6-二溴吡啶相关的问答
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