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About This Item
Linear Formula:
NH4SO3NH2
CAS Number:
Molecular Weight:
114.12
EC Number:
MDL number:
UNSPSC Code:
12352301
PubChem Substance ID:
Recommended Products
grade
JIS special grade
Assay
≥98.5%
form
crystalline
availability
available only in Japan
pH
4.5-6.0 (25 °C, 114.1 g/L)
mp
131-135 °C (lit.)
SMILES string
N.NS(O)(=O)=O
InChI
1S/H3NO3S.H3N/c1-5(2,3)4;/h(H3,1,2,3,4);1H3
InChI key
GEHMBYLTCISYNY-UHFFFAOYSA-N
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Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Cobalt-catalyzed direct arylation and benzylation by C-H/C-O cleavage with sulfamates, carbamates, and phosphates.
Weifeng Song et al.
Angewandte Chemie (International ed. in English), 51(33), 8251-8254 (2012-07-14)
Christopher S Adams et al.
Journal of the American Chemical Society, 134(26), 10807-10810 (2012-06-20)
Nitrogen-containing stereotriads, compounds with three adjacent stereodefined carbons, are commonly found in biologically important molecules. However, the preparation of molecules bearing these motifs can be challenging. Herein, we describe a modular oxidation protocol which converts a substituted allene to a
Laszlo Tarko et al.
Bioorganic & medicinal chemistry, 21(6), 1404-1409 (2012-12-05)
The last version of the PRECLAV algorithm was used to investigate a series of sulfamate/sulfamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. PRECLAV allows identification of outliers for lead hopping, significant molecular fragments and similarity computation of a calibration set vs.
Dengfeng Dou et al.
Bioorganic & medicinal chemistry, 19(20), 5975-5983 (2011-09-20)
A new class of compounds that exhibit anti-norovirus activity in a cell-based system and embody in their structure a cyclosulfamide scaffold has been identified. The structure of the initial hit (compound 2a, ED(50) 4 μM, TD(50) 50 μM) has been
Edward J Emmett et al.
Organic & biomolecular chemistry, 10(20), 4007-4014 (2012-03-13)
By using DABCO·(SO(2))(2), DABSO, as a solid bench-stable SO(2)-equivalent, the palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides has been achieved. N,N-Dialkylhydrazines are employed as the N-nucleophiles and provide N-aminosulfonamides as the products in good to excellent yields. The reactions
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