Formamidinesulfinic acid - CAS 1758-73-2

Catalog:	BB013176
Product Name:	Formamidinesulfinic acid
CAS:	1758-73-2
Synonyms:	amino(imino)methanesulfinic acid

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	amino(imino)methanesulfinic acid
Description:	Formamidinesulfinic acid (CAS# 1758-73-2) is a reagent used in reduction and synthesis reactions.
Molecular Weight:	108.12
Molecular Formula:	CH4N2O2S
Canonical SMILES:	C(=N)(N)S(=O)O
InChI:	InChI=1S/CH4N2O2S/c2-1(3)6(4)5/h(H3,2,3)(H,4,5)
InChI Key:	FYOWZTWVYZOZSI-UHFFFAOYSA-N
Boiling Point:	355.3 ℃ at 760 mmHg
Density:	2.25 g/cm³
Solubility:	Water : 27 g/L at 20 ℃ (68 °F);
Appearance:	White crystalline powder
MDL:	MFCD00002397
LogP:	0.76730

Publication Number	Title	Priority Date
CN-113372489-A	Temperature-sensitive delayed water shutoff agent and preparation method and application thereof	20210812
CN-113481727-A	Organic-inorganic composite antibacterial powder and preparation method thereof	20210805
CN-113501975-A	Functionalized titanium dioxide uvioresistant hydrogel and preparation method thereof	20210729
CN-113480457-A	Production method of high-purity bisphenol S	20210723
CN-113430869-A	Preparation system and method for manufacturing single-sided white board paper by adopting secondary fibers	20210716

PMID	Publication Date	Title	Journal
22840022	20121001	Preparation and characterization of poly(acrylic acid)-hydroxyethyl cellulose graft copolymer	Carbohydrate polymers
21881671	20111021	Thiourea dioxide promoted efficient organocatalytic one-pot synthesis of a library of novel heterocyclic compounds	Organic & biomolecular chemistry
19502160	20090901	Generalized eruption with histopathologic toxic epidermal necrolysis caused by occupational exposure to thiourea dioxide	European journal of dermatology : EJD
19731693	20090801	Elimination of sludge odor by oxidizing sulfur-containing compounds with ferrate(VI)	Environmental science & technology
17266227	20070208	Oxidation and decomposition kinetics of thiourea oxides	The journal of physical chemistry. A

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Related Functional Groups

Sulfur Compounds

[91125-43-8]
Sulfophenyl nonanoate sodium salt
[6633-90-5]
1,4-Butanedithiol diacetate
[1005626-64-1]
3-(1,3-Dimethylpyrazol-4-yl)-5-[(1-methylpyrazol-4-yl)methylidene]-2-sulfanylideneimidazolidin-4-one
[72799-34-9]
3-(2-Ethoxyphenyl)-2-Thioxoimidazolidin-4-One
[2039-96-5]
3-(Trimethylsilyl)-1-propanesulfonic acid sodium salt
[874-87-3]
4-(Methylthio)benzyl chloride

GHS Hazard Statement:	H251 (50.81%): Self-heating; may catch fire [Danger Self-heating substances and mixtures]
Precautionary Statement:	P235+P410, P260, P261, P264, P270, P271, P280, P284, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P310, P312, P314, P320, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P407, P413, P420, and P501
Signal Word:	Danger

Complexity:	89.5
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	107.99934855
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	3
Isotope Atom Count:	0
Monoisotopic Mass:	107.99934855
Rotatable Bond Count:	1
Topological Polar Surface Area:	106 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-1.1