279706
1,1-Bis(methylthio)-2-nitroethylene
95%
Synonym(s):
Nitroketene dimethyl mercaptal
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About This Item
Linear Formula:
O2NCH=C(SCH3)2
CAS Number:
Molecular Weight:
165.23
Beilstein:
1524538
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
95%
form
solid
mp
125-127 °C (lit.)
functional group
amine
nitro
thioether
SMILES string
CS\C(SC)=C/[N+]([O-])=O
InChI
1S/C4H7NO2S2/c1-8-4(9-2)3-5(6)7/h3H,1-2H3
InChI key
NXGHEDHQXXXTTP-UHFFFAOYSA-N
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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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)
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)
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
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