ニトロブロモメタン

Methane, bromonitro-

HCID 68423CAS 563-70-2

データを補完しています。通常は 1 分以内に完了します

基本情報

標準SMILES
O=[N+]([O-])CBr
InChIKey
DNPRVXJGNANVCZ-UHFFFAOYSA-N
分子式
CH2BrNO2
平均分子量
139.936 g/mol
単同位体質量
138.9268904

名称と識別子

優先名称
Methane, bromonitro-
IUPAC
Bromo(nitro)methane
現地名
ニトロブロモメタン
英語名
Bromonitromethane
分子式
CH2BrNO2
分子量
139.94

名称と別名

ブロモニトロメタンニトロブロモメタンニトロメチルブロミドブロモ(ニトロ)メタン255858_ALDRICHEINECS 209-258-0bromonitro-methannitrobromomethaneBROMONITROMETHANENitromethyl bromideMethane, bromonitro-Bromonitromethane, tech.
名称をさらに表示
bromonitromethane CH2BrNO2Bromonitromethane, 90%,tech.

データベース識別子

CAS
563-70-2
PubChem CID
68423
DTXSID
DTXSID7060338
ChEMBL
CHEMBL2335229
UNII
EG63P9EUR0
EC Number
209-258-0
Nikkaji
J435I

物性

物理化学的性質

融点
-28 °C · -28 °C
沸点
146 · 146-148 °C/750 mmHg (lit.)
比重(密度)
2.007 g/mL · 2.007 g/mL at 25 °C (lit.)
屈折率
1.485 · 1.485-1.495
闪点
4 °C · 4°C
貯蔵温度
2 · Storage temp. 2-8°C
化学的性質 · 1 件

化学的特性Bromonitromethane is a clear yellow liquid, It is a strong oxidizing agent with properties similar to nitromethane. Bromonitromethane has been used: in production of various protected α-bromo nitroalkane donors (including Fmoc) for use in Umpolung amide synthesis. in preparation of (Z)-1-bromo-1-nitroalkenes via sodium iodide-catalyzed Henry reaction. in diastereo- and enantioselective cyclopropanation of β,γ-unsaturated a-ketoesters via domino Michael-addition/intramolecular-alkylation strategy.

安全と法規制

安全データ

wgk
3
tsca
TSCA listed
rtecs
PA5360000
ridadr
3098
hs_code
29049095
risk_code
8-36/37/38-20/21/22

化学と産業

応用分野 · 1 件

使用Bromonitromethane has received considerable attention as a one-carbon synthon for the synthesis of a variety of important organic intermediates. Bromonitromethane is a key starting material for the preparation of the broad-spectrum antibiotic trovafloxacin, which contains the interesting 3-azabicyclo[ 3.1.0]hexane ring system. it was used in the synthesis of 2-nitrobenzofuran and 2-nitro-2,3-dihydrobenzofuran-3-ols, nitrobenzo­thio-phenes, and nitrothiazoles, polyfunctionalized nitrocyclopropanes. It has also been utilized in the synthesis of 1-bromo-1-nitroalkan-2-ols and aryl nitromethanes. In addition, it could be used as a bromine donor.

調製方法 · 1 件

製造方法Bromonitromethane is commercially available and can also be easily prepared according to the procedures reported by Fishwick et al. A typical procedure is as following: freshly distilled nitromethane was stirred at 0℃ and bromine was dropped in 5 seconds. The resulted bromonitromethane could be used without further purification.

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関連反応

27 件

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