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| CAS No.: | 3144-09-0 |
|---|---|
| Name: | Methanesulfonamide |
| Molecular Structure: | |
|
|
|
| Formula: | CH5NO2S |
| Molecular Weight: | 95.1222 |
| Synonyms: | Mesylamide;Methanesulfonic amide;Methanesulphonamide;NSC 191039;NSC271; |
| EINECS: | 221-553-6 |
| Density: | 1.363 g/cm3 |
| Melting Point: | 85-89 °C(lit.) |
| Boiling Point: | 208.2 °C at 760 mmHg |
| Flash Point: | 79.7 °C |
| Appearance: | white to yellow crystals, powder or flakes |
| Hazard Symbols: |
Xi
|
| Risk Codes: | 36/37/38 |
| Safety: | 26-36-24/25 |
| PSA: | 68.54000 |
| LogP: | 0.68580 |

| Conditions | Yield |
|---|---|
| With ammonia In dichloromethane for 0.0833333h; | A n/a B 100% |

N-(3-methylbut-2-en-1-yl)methanesulfonamide


methanesulfonamide

| Conditions | Yield |
|---|---|
| With silver hexafluoroantimonate In 1,2-dichloro-ethane at 140℃; for 0.0333333h; Inert atmosphere; Microwave irradiation; | 100% |

| Conditions | Yield |
|---|---|
| With triethylamine In dichloromethane; ethyl acetate | 99% |
| With triethylamine In dichloromethane | 98% |
| 97% |


methanesulfonamide

| Conditions | Yield |
|---|---|
| With silver hexafluoroantimonate In 1,2-dichloro-ethane at 140℃; for 0.0333333h; Microwave irradiation; Inert atmosphere; | 98% |

| Conditions | Yield |
|---|---|
| With triethylamine In dichloromethane; water | 95.6% |
| With triethylamine In dichloromethane; water | 95.6% |
| With triethylamine In dichloromethane; water |


Methanesulfonyl azide


methanesulfonamide

| Conditions | Yield |
|---|---|
| With benzyltriethylammonium tetrathiomolybdate In water; acetonitrile at 25℃; for 0.1h; | 95% |
| With zinc In methanol at 20℃; for 2h; | 92% |
| With iron In water at 20℃; for 2h; Inert atmosphere; | 87% |


methanesulfonamide

| Conditions | Yield |
|---|---|
| With silver hexafluoroantimonate In 1,2-dichloro-ethane at 140℃; for 0.0333333h; Microwave irradiation; Inert atmosphere; | 81% |

tert-butylsulfinyl chloride


N-hydroxylmethanesulfonamide

A

methanesulfonamide

B

di-tert-butyl thiosulfonate

C

trifluoromethane sulfonic anhydride

D

C5H13NO4S2

| Conditions | Yield |
|---|---|
| With pyridine In acetone at 20℃; for 2h; Mechanism; Product distribution; other N-hydroxy sulfonamides; | A 80% B 13% C 22% D 15% |



methanesulfonamide

| Conditions | Yield |
|---|---|
| With hydrazine hydrate In ethanol at 20℃; for 2h; | 80% |

N-methanesulfonyl-3-phenylpropylamine

A

3-phenyl-propionaldehyde

B

methanesulfonamide

C

3-(4-iodophenyl)propionaldehyde

| Conditions | Yield |
|---|---|
| With [bis(acetoxy)iodo]benzene; iodine In 1,2-dichloro-ethane at 30 - 40℃; for 3h; ultrasonic irradiation; | A 24% B 66% C 39% |

