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经验公式(希尔记法):
C16H24Cl2Ir2
化学文摘社编号:
分子量:
671.70
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
235-170-7
MDL number:
产品名称
HS157, Umicore, 97%
InChI
1S/2C8H12.2ClH.2Ir/c2*1-2-4-6-8-7-5-3-1;;;;/h2*1-2,7-8H,3-6H2;2*1H;;/q;;;;2*+1/p-2/b2*2-1-,8-7-;;;;
InChI key
ZFOUDQNHNLDNLD-MIXQCLKLSA-L
SMILES string
Cl[Ir].Cl[Ir].C1CC=CCCC=C1.C2CC=CCCC=C2
assay
97%
form
powder
reaction suitability
core: iridium
reaction type: C-H Activation
reagent type: catalyst
mp
205 °C (dec.) (lit.)
Quality Level
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Application
Legal Information
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
P A Marks et al.
Journal of the National Cancer Institute, 92(15), 1210-1216 (2000-08-03)
Histone deacetylase (HDAC) inhibitors have been shown to be potent inducers of growth arrest, differentiation, and/or apoptotic cell death of transformed cells in vitro and in vivo. One class of HDAC inhibitors, hydroxamic acid-based hybrid polar compounds (HPCs), induce differentiation
商品
Arylboronic acids and esters, vital tools in chemical transformations, find extensive use, particularly in the Suzuki-Miyaura cross-coupling reaction.
Precatalysts for asymmetric catalysis offer batch-to-batch consistency in a range of catalytic reactions, supporting diverse research needs.
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