Product Name

  • Name

    2-AMINO-ETHANESULFONAMIDE

  • EINECS 1308068-626-2
  • CAS No. 4378-70-5
  • Article Data9
  • CAS DataBase
  • Density 1.38 g/cm3
  • Solubility
  • Melting Point 90-100 °C
  • Formula C2H8N2O2S
  • Boiling Point 303.7 °C at 760 mmHg
  • Molecular Weight 124.164
  • Flash Point 137.5 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 4378-70-5 (2-AMINO-ETHANESULFONAMIDE)
  • Hazard Symbols IrritantXi
  • Synonyms 2-Aminoethanesulfonamide;2-Sulfamoylethylamine;Aminoethanesulfonamide;NSC 403678;Taurinamide;
  • PSA 94.56000
  • LogP 1.51700

Synthetic route

N-carbobenzoxy-β-aminoethanesulfonamide
136027-17-3

N-carbobenzoxy-β-aminoethanesulfonamide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

Conditions
ConditionsYield
With methanol; palladium; acetic acid durch Hydrogenolyse;
With formic acid; hydrogen; palladium on activated charcoal In methanol
2-phthalimidoethane sulfonamide
4443-23-6

2-phthalimidoethane sulfonamide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

Conditions
ConditionsYield
With hydrazine hydrate In ethanol
With water; hydrazine In ethanol for 3h; Reflux;
2-benzamino-ethane-sulfonic acid-(1)-amide

2-benzamino-ethane-sulfonic acid-(1)-amide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

Conditions
ConditionsYield
With hydrogenchloride
2-phthalimido-ethane-sulfonic acid-(1)-amide

2-phthalimido-ethane-sulfonic acid-(1)-amide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

Conditions
ConditionsYield
With ethanol; hydrazine hydrate Erhitzen des Reaktionsprodukts mit wss.HCl;
Taurultam

Taurultam

A

formaldehyd
50-00-0

formaldehyd

B

dehydrotaurultam

dehydrotaurultam

C

Tau
107-35-7

Tau

D

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

E

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
With water Product distribution / selectivity; γ-Irradiation;
...Expand
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

2,6-dichlorophenylisothiocyanate
6590-95-0

2,6-dichlorophenylisothiocyanate

2-[3-(2,6-Dichloro-phenyl)-thioureido]-ethanesulfonic acid amide
75257-76-0

2-[3-(2,6-Dichloro-phenyl)-thioureido]-ethanesulfonic acid amide

Conditions
ConditionsYield
Ambient temperature;91%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

C22H34Cl2N4O2

C22H34Cl2N4O2

C24H41ClN6O4S

C24H41ClN6O4S

Conditions
ConditionsYield
With triethylamine In butan-1-ol at 85 - 90℃; for 4h;79%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

3-(4-benzyloxy-3-bromo-phenyl)-2-[(Z)-benzyloxyimino]-propionic acid

3-(4-benzyloxy-3-bromo-phenyl)-2-[(Z)-benzyloxyimino]-propionic acid

(E)-3-(4-(benzyloxy)-3-bromophenyl)-2-(benzyloxyimino)-N-(2-sulfamoylethyl)propanamide
1415814-15-1

(E)-3-(4-(benzyloxy)-3-bromophenyl)-2-(benzyloxyimino)-N-(2-sulfamoylethyl)propanamide

Conditions
ConditionsYield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In 1,4-dioxane; methanol at 20℃; Inert atmosphere;69%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐nitro‐1,2,5‐oxadiazol‐3‐yl)‐4,5‐dihydro‐1,2,4‐oxadiazol‐5‐one

4‐(3‐bromo‐4‐fluorophenyl)‐3‐(4‐nitro‐1,2,5‐oxadiazol‐3‐yl)‐4,5‐dihydro‐1,2,4‐oxadiazol‐5‐one

2-((4-(4-(3-bromo-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl )-1,2,5-oxadiazol-3-yl)amino)ethanesulfonamide

2-((4-(4-(3-bromo-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl )-1,2,5-oxadiazol-3-yl)amino)ethanesulfonamide

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 20℃; for 2h;50.7%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

4-acetylisoquinolin-1(2H)-one
87275-00-1

4-acetylisoquinolin-1(2H)-one

2-(1-(1-oxo-1,2-dihydroisoquinolin-4-yl)ethylamino)ethanesulfonamide

2-(1-(1-oxo-1,2-dihydroisoquinolin-4-yl)ethylamino)ethanesulfonamide

Conditions
ConditionsYield
Stage #1: 2-aminoethanesulfonamide; 4-acetylisoquinolin-1(2H)-one With titanium(IV) isopropylate In tetrahydrofuran at 20℃; for 6h; Inert atmosphere;
Stage #2: With sodium tetrahydroborate; ethanol In tetrahydrofuran at 0 - 20℃; for 2h;		50%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

(+)-usnic acid
17669-01-1, 56190-51-3, 15853-98-2

(+)-usnic acid

(R,E)-2-(1-(6-acetyl-7,9-dihydroxy-8,9b-dimethyl-1,3-dioxo-1,9b-dihydrodibenzo[b,d]furan-2(3H)-ylidene)-ethylamino)ethanesulfonamide

(R,E)-2-(1-(6-acetyl-7,9-dihydroxy-8,9b-dimethyl-1,3-dioxo-1,9b-dihydrodibenzo[b,d]furan-2(3H)-ylidene)-ethylamino)ethanesulfonamide

Conditions
ConditionsYield
With triethylamine In ethanol for 1h; Reflux; regioselective reaction;48%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

3-(3-(4-chloro-5-fluoropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazol-5-yl)isoxazole
1446358-48-0

3-(3-(4-chloro-5-fluoropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazol-5-yl)isoxazole

C19H17F2N7O3S

C19H17F2N7O3S

Conditions
ConditionsYield
With triethylamine In 1,4-dioxane at 65℃; for 24h;42%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl (2-sulfamoylethyl)carbamate
1375279-51-8

tert-butyl (2-sulfamoylethyl)carbamate

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane at 20℃; for 16h;30%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

C17H18F2N6O3S

C17H18F2N6O3S

Conditions
ConditionsYield
With triethylamine In 1,4-dioxane at 90℃;23%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

6-formyl-N-(2-methyl-[1,1'-biphenyl]-3-yl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

6-formyl-N-(2-methyl-[1,1'-biphenyl]-3-yl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

N-(2-methyl-[1,1'-biphenyl]-3-yl)-6-(((2-sulfamoylethyl)amino)methyl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

N-(2-methyl-[1,1'-biphenyl]-3-yl)-6-(((2-sulfamoylethyl)amino)methyl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

Conditions
ConditionsYield
Stage #1: 2-aminoethanesulfonamide; 6-formyl-N-(2-methyl-[1,1'-biphenyl]-3-yl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide With acetic acid In N,N-dimethyl-formamide at 20℃; for 1h;
Stage #2: With sodium cyanoborohydride In N,N-dimethyl-formamide at 20℃;		23%
Stage #1: 2-aminoethanesulfonamide; 6-formyl-N-(2-methyl-[1,1'-biphenyl]-3-yl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide With acetic acid In N,N-dimethyl-formamide at 20℃; for 2h;
Stage #2: In N,N-dimethyl-formamide at 25℃; for 12h;
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

C17H14N4O6

C17H14N4O6

C19H20N6O7S

C19H20N6O7S

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl acetamide at 20℃; for 72h;20.7%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

C17H14N4O6

C17H14N4O6

C19H20N6O7S

C19H20N6O7S

Conditions
ConditionsYield
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In N,N-dimethyl acetamide at 20℃; for 72h;20.7%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

2-{[5-bromo-1-(2-chlorophenyl)-1H-1,2,4-triazol-3-yl]methyl}-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

2-{[5-bromo-1-(2-chlorophenyl)-1H-1,2,4-triazol-3-yl]methyl}-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one

2-{[1-(2-chlorophenyl)-3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-5-yl]amino}ethanesulfonamide

2-{[1-(2-chlorophenyl)-3-({3-(4-chlorophenyl)-5-oxo-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-4,5-dihydro-1H-1,2,4-triazol-1-yl}methyl)-1H-1,2,4-triazol-5-yl]amino}ethanesulfonamide

Conditions
ConditionsYield
Stage #1: 2-aminoethanesulfonamide; 2-{[5-bromo-1-(2-chlorophenyl)-1H-1,2,4-triazol-3-yl]methyl}-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one With N-ethyl-N,N-diisopropylamine In acetonitrile at 150 - 180℃; for 19h; Microwave irradiation;
Stage #2: 2-aminoethanesulfonamide at 200℃; for 2h;		12%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

cis-1-(4-fluoro-benzyl)-4-hydroxy-3-(7-iodo-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-1,4a,5,6,7,7a-hexahydro-[1]pyrindin-2-one

cis-1-(4-fluoro-benzyl)-4-hydroxy-3-(7-iodo-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-3-yl)-1,4a,5,6,7,7a-hexahydro-[1]pyrindin-2-one

cis-2-amino-ethanesulfonic acid {3-[1-(4-fluoro-benzyl)-4-hydroxy-2-oxo-2,4a,5,6,7,7a-hexahydro-1H-[1]pyrindin-3-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-amide

cis-2-amino-ethanesulfonic acid {3-[1-(4-fluoro-benzyl)-4-hydroxy-2-oxo-2,4a,5,6,7,7a-hexahydro-1H-[1]pyrindin-3-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[1,2,4]thiadiazin-7-yl}-amide

Conditions
ConditionsYield
With potassium phosphate; copper(l) iodide; sarcosine In N,N-dimethyl-formamide at 100 - 120℃; for 3.5h;10%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

5-hydroxy-4-(7-iodo-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-3-yl)-2-(3-methyl-butyl)-6-thiophen-2-yl-2H-pyridazin-3-one
1038403-26-7

5-hydroxy-4-(7-iodo-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-3-yl)-2-(3-methyl-butyl)-6-thiophen-2-yl-2H-pyridazin-3-one

A

2-(3-[5-hydroxy-2-(3-methyl-butyl)-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,2-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-ylamino)-ethanesulfonic acid amide
1038402-99-1

2-(3-[5-hydroxy-2-(3-methyl-butyl)-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,2-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-ylamino)-ethanesulfonic acid amide

B

2-amino-ethanesulfonic acid {3-[5-hydroxy-2-(3-methyl-butyl)-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}amide
1038402-98-0

2-amino-ethanesulfonic acid {3-[5-hydroxy-2-(3-methyl-butyl)-3-oxo-6-thiophen-2-yl-2,3-dihydro-pyridazin-4-yl]-1,1-dioxo-1,4-dihydro-1λ6-benzo[e][1,2,4]thiadiazin-7-yl}amide

Conditions
ConditionsYield
With potassium phosphate; sarcosine; copper(l) iodide In N,N-dimethyl-formamide at 100℃; for 3h;A 9%
B 8.7%
...Expand
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

(+/-)-(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acid

(+/-)-(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acid

(3S,3aR)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-N-(2-sulfamoylethyl)-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxamide
1023653-78-2

(3S,3aR)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-N-(2-sulfamoylethyl)-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxamide

Conditions
ConditionsYield
Stage #1: (+/-)-(3SR,3aRS)-2-(3-chloro-4-cyanophenyl)-3-cyclopentyl-3,3a,4,5-tetrahydro-2H-benzo[g]indazole-7-carboxylic acid With benzotriazol-1-ol; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine In N,N-dimethyl-formamide for 0.25h;
Stage #2: 2-aminoethanesulfonamide In N,N-dimethyl-formamide at 20℃; for 20h;		8%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

(S)-3-(3-(((R)-4-ethyl-1,1-dioxido-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl)methyl)-4-methylphenyl)-3-(1-ethyl-4-methyl-1H-benzo[d][1,2,3]triazol-5-yl)propanoic acid

(S)-3-(3-(((R)-4-ethyl-1,1-dioxido-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl)methyl)-4-methylphenyl)-3-(1-ethyl-4-methyl-1H-benzo[d][1,2,3]triazol-5-yl)propanoic acid

(S)-3-(3-(((R)-4-ethyl-1,1-dioxido-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl)methyl)-4-methylphenyl)-3-(1-ethyl-4-methyl-1H-benzo[d][1,2,3]triazol-5-yl)-N-(2-sulfamoylethyl)propanamide

(S)-3-(3-(((R)-4-ethyl-1,1-dioxido-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl)methyl)-4-methylphenyl)-3-(1-ethyl-4-methyl-1H-benzo[d][1,2,3]triazol-5-yl)-N-(2-sulfamoylethyl)propanamide

Conditions
ConditionsYield
Stage #1: (S)-3-(3-(((R)-4-ethyl-1,1-dioxido-3,4-dihydro-2H-pyrido[2,3-b][1,4,5]oxathiazepin-2-yl)methyl)-4-methylphenyl)-3-(1-ethyl-4-methyl-1H-benzo[d][1,2,3]triazol-5-yl)propanoic acid With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide for 0.05h;
Stage #2: 2-aminoethanesulfonamide In N,N-dimethyl-formamide at 20℃; for 18h; Sealed tube;		6.32%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

N-(3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-methylphenyl)-6-formyl-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

N-(3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-methylphenyl)-6-formyl-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

N-(3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-methylphenyl)-6-(((2-sulfamoylethyl)amino)methyl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

N-(3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-methylphenyl)-6-(((2-sulfamoylethyl)amino)methyl)-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide

Conditions
ConditionsYield
Stage #1: 2-aminoethanesulfonamide; N-(3-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-2-methylphenyl)-6-formyl-[1,2,4]triazolo[4,3-a]pyridine-8-carboxamide With acetic acid In N,N-dimethyl-formamide at 20℃; for 1h;
Stage #2: With sodium cyanoborohydride In N,N-dimethyl-formamide at 20℃;		6%
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

pantolactone
79-50-5

pantolactone

2-pantoylamino-ethanesulfonic acid amide
51026-57-4

2-pantoylamino-ethanesulfonic acid amide

Conditions
ConditionsYield
at 120℃;
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

4-(4-nitrophenoxy)butanoic acid
28341-54-0

4-(4-nitrophenoxy)butanoic acid

2-(4-hydroxy-butyrylamino)-ethanesulfonic acid amide

2-(4-hydroxy-butyrylamino)-ethanesulfonic acid amide

Conditions
ConditionsYield
at 120℃;
potassium cyanate
590-28-3

potassium cyanate

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

2-ureido-ethanesulfonic acid amide
89034-20-8

2-ureido-ethanesulfonic acid amide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

acetic anhydride
108-24-7

acetic anhydride

2-acetylamino-ethanesulfonic acid acetylamide

2-acetylamino-ethanesulfonic acid acetylamide

2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

4-Nitrobenzenesulfonyl chloride
98-74-8

4-Nitrobenzenesulfonyl chloride

2-(4-nitro-benzenesulfonylamino)-ethanesulfonic acid amide

2-(4-nitro-benzenesulfonylamino)-ethanesulfonic acid amide

Conditions
ConditionsYield
With sodium carbonate
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

(R)-Pantolacton
599-04-2

(R)-Pantolacton

2-pantoylamino-ethanesulfonic acid amide; (N-D-pantoyl-taurin)-amide
51250-35-2

2-pantoylamino-ethanesulfonic acid amide; (N-D-pantoyl-taurin)-amide

Conditions
ConditionsYield
at 100 - 110℃;
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

2-acetoxy-2-phenylacetyl chloride
1638-63-7

2-acetoxy-2-phenylacetyl chloride

acetoxy-phenyl-acetic acid-(2-sulfamoyl-ethylamide)

acetoxy-phenyl-acetic acid-(2-sulfamoyl-ethylamide)

Conditions
ConditionsYield
With water; sodium hydrogencarbonate
2-aminoethanesulfonamide
4378-70-5

2-aminoethanesulfonamide

(2S,4S)-4-Acetylsulfanyl-2-ethoxycarbonyloxycarbonyl-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

(2S,4S)-4-Acetylsulfanyl-2-ethoxycarbonyloxycarbonyl-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

(2S,4S)-4-Acetylsulfanyl-2-(2-sulfamoyl-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester
212608-03-2

(2S,4S)-4-Acetylsulfanyl-2-(2-sulfamoyl-ethylcarbamoyl)-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

Conditions
ConditionsYield
In tetrahydrofuran at 0℃; Yield given;

Ethanesulfonamide,2-amino- Specification

The Ethanesulfonamide,2-amino-, also known as Aminoethanesulfonamide, is the organic compound with the formula C2H8N2O2S. With the CAS registry number 4378-70-5, its IUPAC name is 2-aminoethanesulfonamide. When you are using this chemical, you shoule be very cautious. Because it may cause inflammation to the skin or other mucous membranes.

Physical properties of Ethanesulfonamide,2-amino-: (1)XLogP3-AA: -2; (2)H-Bond Donor: 2; (3)H-Bond Acceptor: 4; (4)Rotatable Bond Count: 2; (5)Exact Mass: 124.030648; (6)MonoIsotopic Mass: 124.030648; (7)Topological Polar Surface Area: 94.6; (8)Heavy Atom Count: 7; (9)Formal Charge: 0; (10)Complexity: 121; (11)Isotope Atom Count: 0; (12)Covalently-Bonded Unit Count: 1.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C(CS(=O)(=O)N)N
(2)InChI: InChI=1S/C2H8N2O2S/c3-1-2-7(4,5)6/h1-3H2,(H2,4,5,6)
(3)InChIKey: MVQXBXLDXSQURK-UHFFFAOYSA-N

Related Products

Hot Products

Post buying leads

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View