279706
1,1-双(甲硫基)-2-硝基乙烯
95%
别名:
硝基乙烯酮二甲基缩硫醛
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关于此项目
线性分子式:
O2NCH=C(SCH3)2
化学文摘社编号:
分子量:
165.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
237-108-4
Beilstein/REAXYS Number:
1524538
MDL number:
Assay:
95%
Form:
solid
产品名称
1,1-双(甲硫基)-2-硝基乙烯, 95%
InChI key
NXGHEDHQXXXTTP-UHFFFAOYSA-N
InChI
1S/C4H7NO2S2/c1-8-4(9-2)3-5(6)7/h3H,1-2H3
SMILES string
CS\C(SC)=C/[N+]([O-])=O
assay
95%
form
solid
mp
125-127 °C (lit.)
functional group
amine
nitro
thioether
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
法规信息
新产品
此项目有
Synthesis of the novel pyrimido[1,6-a]pyrimidine and imidazo[1,2-c]pyrimidine derivatives based on heterocyclic ketene aminals.
Alizadeh A, et al.
Tetrahedron, 68(1), 319-322 (2012)
Nasrin Zohreh et al.
ACS combinatorial science, 15(6), 278-286 (2013-04-30)
A previously unknown class of highly substituted pyridazines and pyrazoline-spirooxinoles are easily prepared by an uncatalyzed one-pot three-component approach incorporating a domino SN/condensation/aza-ene addition cyclization reaction sequence. 1,1-Dihydrazino-2-nitroethylene (DHNE) which is generated in situ from the nucleophilic substitution (SN) reaction
Efficient one-pot synthesis of spirooxindole derivatives containing 1, 4-dihydropyridine-fused-1, 3-diazaheterocycle fragments via four-component reaction.
Alizadeh A, et al.
Synthesis, 2010(22), 3913-3917 (2010)
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