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About This Item
经验公式（希尔记法）:
C10H16O2
CAS号:
分子量:
168.23
MDL號碼:
分類程式碼代碼:
12352300
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
96%
形狀
liquid
反應適用性
reagent type: ligand
折射率
n20/D 1.5006
密度
1.0076 g/mL at 25 °C
官能基
ketone
SMILES 字串
CC(C)C(=O)C1CCCCC1=O
InChI
1S/C10H16O2/c1-7(2)10(12)8-5-3-4-6-9(8)11/h7-8H,3-6H2,1-2H3
InChI 密鑰
PFOYYSGBGILOQZ-UHFFFAOYSA-N
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
219.9 °F - closed cup
閃點（°C）
104.4 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
An alternative to the classical α-arylation: the transfer of an intact 2-iodoaryl from ArI(O₂CCF₃)₂.
Zhiyu Jia et al.
Angewandte Chemie (International ed. in English), 53(42), 11298-11301 (2014-09-10)
The α-arylation of carbonyl compounds is generally accomplished under basic conditions, both under metal catalysis and via aryl transfer from the diaryl λ(3)-iodanes. Here, we describe an alternative metal-free α-arylation using ArI(O2CCF3)2 as the source of a 2-iodoaryl group. The
商品
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
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