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About This Item
經驗公式(希爾表示法):
C4H2BrIN2
CAS號碼:
分子量::
284.88
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推薦產品
化驗
97%
形狀
solid
mp
99-103 °C (lit.)
官能基
bromo
iodo
SMILES 字串
Brc1cnc(I)nc1
InChI
1S/C4H2BrIN2/c5-3-1-7-4(6)8-2-3/h1-2H
InChI 密鑰
ZEZKXPQIDURFKA-UHFFFAOYSA-N
一般說明
5-Bromo-2-iodopyrimidine can be synthesized by reacting 5-bromo-2-chloropyrimidine with hydroiodic acid.
應用
5-Bromo-2-iodopyrimidine can be used to synthesize 5,5′-dibromo-2,2′-bipyrimidine and O,O′-dimethyl hyrtinadine A.
訊號詞
Danger
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
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
"One-Pot Synthesis of Diazine-Bridged Bisindoles and Concise Synthesis of the Marine Alkaloid Hyrtinadine A"
Tasch.O.A.B, et al.
European Journal of Organic Chemistry, 2011(24), 4532-4535 (2011)
Gábor Vlád et al.
The Journal of organic chemistry, 67(18), 6550-6552 (2002-08-31)
A high-yield synthesis was developed for the preparation of 2,2'-bipyrimidine (1) using the Ullmann coupling of 2-iodopyrimidine. The new procedure was also used for the preparation of 4,4',6,6'-tetramethyl-2,2'-bipyrimidine (2) and 5,5'-dibromo-2,2'-bipyrimidine (3).
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