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Merck
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220051

Sigma-Aldrich

N-碘代琥珀酰亚胺

95%

别名:

1-iodo-pyrrolidine-2,5-dione, 1-iodoazolidine-2,5-dione, NIS, succiniodimide

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About This Item

经验公式（希尔记法）:
C4H4INO2
CAS号:
516-12-1
分子量:
224.98
Beilstein:
113917
EC 号:
208-221-6
MDL编号:
MFCD00005512
UNSPSC代码:
12352101
PubChem化学物质编号:
24853162
NACRES:
NA.22

质量水平

200

方案

95%

表单

powder

mp

202-206 °C (lit.)

官能团

imide

储存温度

2-8°C

SMILES字符串

IN1C(=O)CCC1=O

InChI

1S/C4H4INO2/c5-6-3(7)1-2-4(6)8/h1-2H2

InChI key

LQZMLBORDGWNPD-UHFFFAOYSA-N

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应用

从 1,6-二炔经过高效的两步工艺制备的高取代的碘苯。与 TFA 一起使用，将硫苷化学选择性地水解为 1-羟基糖苷。从烯烃和苯亚磺酸合成乙烯砜。

警示用语：

Warning

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1B

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCJ8150
BCCF4767
BCBZ9619
BCBT9406
BCBR1588V

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Highly substituted iodobenzenes were efficiently and regioselectively synthesized from readily available 1,6-diynes via two-step process consisting of silver-catalyzed Csp-H iodination and subsequent ruthenium-catalyzed [2 + 2 + 2] cycloaddition of resultant iododiynes. Some of the obtained iodobenzenes were subjected to
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