cetylpyridinium chloride
sodium 4-aminobenzenesulfonylacetamide
hexadecylpyridinium sulfacetamide
Conditions | Yield |
---|---|
In water for 0.5h; Heating / reflux; | 99.22% |
4-(4-fluorophenyl)-4-oxo-2-hydroxy-2-butenoic acid methyl ester
sodium 4-aminobenzenesulfonylacetamide
2-hydroxy-4-oxo-4-(4-fluorophenyl)-2-butenoic acid N-(4-(acetylaminosulfonyl)phenyl)amide
Conditions | Yield |
---|---|
With acetic acid Reflux; | 95% |
chloroformic acid ethyl ester
sodium 4-aminobenzenesulfonylacetamide
C11H14N2O5S
Conditions | Yield |
---|---|
Ambient temperature; | 91.5% |
sodium 4-aminobenzenesulfonylacetamide
chloroacetic acid ethyl ester
N-Sulfanilyl-N-carbethoxymethylacetamine
Conditions | Yield |
---|---|
In ethanol for 4h; Ambient temperature; | 89.7% |
sodium 4-aminobenzenesulfonylacetamide
Conditions | Yield |
---|---|
In methanol; water at 20℃; for 2h; | 88% |
sodium 4-aminobenzenesulfonylacetamide
N,N-didecyl-N,N-dimethylammonium bromide
didecyldimethylammonium sulfacetamide
Conditions | Yield |
---|---|
In water for 0.5h; | 87.74% |
sodium 4-aminobenzenesulfonylacetamide
methyl chloroacetate
[Acetyl-(4-amino-benzenesulfonyl)-amino]-acetic acid methyl ester
Conditions | Yield |
---|---|
Ambient temperature; | 87.5% |
Conditions | Yield |
---|---|
Ambient temperature; | 85.8% |
sodium 4-aminobenzenesulfonylacetamide
4,6-dichloro-5-methoxypyrimidine
4-(p-aminobenzenesulfonamido)-5-methoxy-6-chloropyrimidine
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 88 - 90℃; for 3h; | 85.3% |
C11H8Cl2O4
sodium 4-aminobenzenesulfonylacetamide
2-hydroxy-4-(2,4-dichlorophenyl)-4-oxo-2-butenoic acid N-(4-acetylaminosulfonylphenyl)amide
Conditions | Yield |
---|---|
With acetic acid Reflux; | 83% |
Conditions | Yield |
---|---|
In methanol; water at 20℃; for 2h; | 83% |
sodium 4-aminobenzenesulfonylacetamide
2-hydroxy-4-(3-methoxyphenyl)-4-oxo-2-butenoic acid N-(4-acetylaminosulfonylphenyl)amide
Conditions | Yield |
---|---|
With acetic acid Reflux; | 81% |
sodium 4-aminobenzenesulfonylacetamide
chloroacetic acid
[Acetyl-(4-amino-benzenesulfonyl)-amino]-acetic acid
Conditions | Yield |
---|---|
80.3% |
4-(4-chlorophenyl)-2-hydroxy-4-oxo-but-2-enoic acid methyl ester
sodium 4-aminobenzenesulfonylacetamide
2-hydroxy-4-oxo-4-(4-chlorophenyl)-2-butenoic acid N-(4-acetylaminosulfonylphenyl)amide
Conditions | Yield |
---|---|
With acetic acid Reflux; | 79% |
2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid methyl ester
sodium 4-aminobenzenesulfonylacetamide
2-hydroxy-4-oxo-4-phenyl-2-butenoic acid N-(4-acetylaminosulfonylphenyl)amide
Conditions | Yield |
---|---|
With acetic acid Reflux; | 76% |
6,8-dibromo-2-phenyl-3,1-benzoxazin-4-one
sodium 4-aminobenzenesulfonylacetamide
Conditions | Yield |
---|---|
at 150℃; for 2h; | 75% |
Conditions | Yield |
---|---|
In ethanol for 1h; Reflux; | 72% |
sodium 4-aminobenzenesulfonylacetamide
ranitidine hydrochloride
Conditions | Yield |
---|---|
In water at 40℃; for 24h; | 50% |
sodium 4-aminobenzenesulfonylacetamide
Conditions | Yield |
---|---|
With dipotassium peroxodisulfate In water at 34.9℃; Kinetics; Mechanism; Thermodynamic data; ΔG(excit.), ΔH(excit.), ΔS(excit.); other temperatures, salt effect (K2SO4), pH and dielectric constant dependence, inhibition by diphenyl picryl hydrazyl; |
Conditions | Yield |
---|---|
With Cu(2+)*2HO(1-)*H3IO6(1-)*K(1+) In water at 29.84℃; Kinetics; Mechanism; Temperature; |
Conditions | Yield |
---|---|
In ethanol at 0℃; Mannich Aminomethylation; Reflux; |
Conditions | Yield |
---|---|
In methanol at 60℃; for 2h; |
Conditions | Yield |
---|---|
In methanol at 60℃; for 2h; |
sodium 4-aminobenzenesulfonylacetamide
Conditions | Yield |
---|---|
In methanol; water at 60℃; for 2h; |
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 3 g |
Conditions | Yield |
---|---|
Stage #1: 4-bromo-phenol; triphenylphosphine In ethylene glycol at 180℃; for 5h; Stage #2: sodium 4-aminobenzenesulfonylacetamide In dichloromethane; water at 20℃; for 24h; | 4 g |
Conditions | Yield |
---|---|
In methanol at 60℃; Reflux; |
Conditions | Yield |
---|---|
Stage #1: sodium 4-aminobenzenesulfonylacetamide With hydrogenchloride; sodium nitrite In water at 15℃; Stage #2: 8-hydroxy-7-iodo-quinoline-5-sulfonic acid With ammonium hydroxide In water for 0.166667h; Reagent/catalyst; Time; |
Conditions | Yield |
---|---|
In dichloromethane; water at 20℃; for 24h; | 3 g |
Conditions | Yield |
---|---|
With hydrogenchloride In water pH=2 - 3; |
Reported in EPA TSCA Inventory.
The Sulfacetamide sodium anhydrous, with the CAS registry number 127-56-0,is also known as Sodium sulfacetamide; N-Sulfanilylacetamide monosodium salt; N-(4-Aminophenylsulfonyl)acetamide sodium salt. It belongs to the product categories of Antibiotics for Research and Experimental Use;Biochemistry.Its EINECS number is 204-848-4. This chemical's molecular formula is C8H9N2NaO3S and molecular weight is 236.22. What's more,Its systematic name is Sulfacetamide sodium.It is an anti-infective agent that is used topically to treat skin infections and orally for urinary tract infections. The Sulfacetamide sodium is irritating to eyes, respiratory system and skin.In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.When you use it,you should wear suitable protective clothing.
Physical properties about Sulfacetamide sodium anhydrous are:
(1)ACD/LogP: -0.964; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -1.18; (4)ACD/LogD (pH 7.4): -2.51; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 4.29; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 5; (10)#H bond donors: 3; (11)#Freely Rotating Bonds: 2; (12)Flash Point: 226.4 °C; (13)Enthalpy of Vaporization: 74.79 kJ/mol ; (14)Boiling Point: 450.8 °C at 760 mmHg; (15)Vapour Pressure: 6.51E-09 mmHg at 25°C.
You can still convert the following datas into molecular structure:
(1)SMILES:[Na+].O=S(=O)([N-]C(=O)C)c1ccc(N)cc1;
(2)Std. InChI:InChI=1S/C8H10N2O3S.Na/c1-6(11)10-14(12,13)8-4-2-7(9)3-5-8;/h2-5H,9H2,1H3,(H,10,11);/q;+1/p-1;
(3)Std. InChIKey:PQMSFAORUFMASU-UHFFFAOYSA-M.
The toxicity data of Sulfacetamide sodium anhydrous as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | subcutaneous | 6gm/kg (6000mg/kg) | Arzneimittel-Forschung. Drug Research. Vol. 9, Pg. 286, 1959. | |
mouse | LDLo | intravenous | 800mg/kg (800mg/kg) | Journal of Pharmacology and Experimental Therapeutics. Vol. 77, Pg. 127, 1943. |
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