220051
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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关于此项目
经验公式（希尔记法）:
C4H4INO2
化学文摘社编号:
分子量:
224.98
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-221-6
Beilstein/REAXYS Number:
113917
MDL number:
产品名称
N-碘代琥珀酰亚胺, 95%
InChI key
LQZMLBORDGWNPD-UHFFFAOYSA-N
InChI
1S/C4H4INO2/c5-6-3(7)1-2-4(6)8/h1-2H2
SMILES string
IN1C(=O)CCC1=O
assay
95%
form
powder
mp
202-206 °C (lit.)
functional group
imide
storage temp.
2-8°C
Quality Level
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Application
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。
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1B
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Canadian Journal of Chemistry, 84, 66-66 (2006)
Abby J Isaacs et al.
The Journal of thoracic and cardiovascular surgery, 149(5), 1262-1269 (2015-03-21)
Substantial controversy surrounds the choice between a mechanical versus bioprosthetic prosthesis for aortic valve replacement (AVR), based on age. This study aims to investigate national trends and in-hospital outcomes of the 2 prosthesis choices. All patients aged >18 years in
Earl S Ford
Chest, 147(4), 989-998 (2014-11-07)
Numbers and rates of hospitalizations and ED visits by patients with COPD are important metrics for surveillance purposes. The objective of this study was to examine trends in these rates from 2001 to 2012 among adults aged ≥ 18 years
Yoshihiko Yamamoto et al.
Journal of the American Chemical Society, 128(25), 8336-8340 (2006-06-22)
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
Taichi Kano et al.
Journal of the American Chemical Society, 130(12), 3728-3729 (2008-03-07)
A direct asymmetric iodination reaction of aldehydes with NIS was found to be catalyzed by the novel axially chiral bifunctional amino alcohol (S)-1d. This method represents the rare example of the catalytic and highly enantioselective synthesis of optically active alpha-iodoaldehydes.
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