Detail of > 21896-59-3
- CAS Number:
- 21896-59-3
- Name:
Methanesulfonamide,N-(2-chloroethyl)-
- Formula:
- C3H8ClNO2S
- Molecular Structure:

- Molecular Weight:
- 157.61912
- EINECS:
- 244-641-6
- Density:
- 1.321 g/cm3
- Boiling Point:
- 245.8 °C at 760 mmHg
- Flash Point:
- 102.5 °C
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Reference
- Preparation of sulfonamide derivatives as metal chelators
- Preparation of sulfonamide derivatives as metal chelators. Okada, Hisashi; Yagihara, Morio (Fuji Photo Film Co.Except for chemicals metioned above, 21896-59-3 is also used., Ltd., Japan). Ger. Offen. DE 4142960 A1 2 Jul 1992, 9 pp. (Germany). CODEN: GWXXBX. CLASS: ICM: C07C311-05. ICA: G03C005-30; G01N031-16. APPLICATION: DE 91-4142960 24 Dec 1991. PRIORITY: JP 90-405649 25 Dec 1990.In this experiment, several chemicals are used like 21896-59-3 DOCUMENT TYPE: Patent CA Section: 23 (Aliphatic Compounds) Section cross-reference(s): 54 Sulfonamide derivs. RSO2NHZ1NXY (R = alkyl, XZ2CO2M, WNZZ1HSO2R; Y = RSO2NHZ1, Z2CO2M; Z1, Z2 = alkylene; Z = Y; M = H, cation; X and Y are not simultaneously = Z2CO2M] were prepd. as metal chelators (no data). Thus, 0.42 mol ClCH2CH2NHSO2Me and 0.42 mol 5N NaOH were added to a soln. of 0.20 mol glycine in 0.20 mol 5N NaOH at 50°. The soln. was stirred 5 h at 50 to give (MeSO2NHCH2CH2)2NCH2CO2H in 32% yield. ..
- Preparation of sulfonamide derivatives as metal chelators
- Preparation of sulfonamide derivatives as metal chelators. Okada, Hisashi; Yagihara, Morio (Fuji Photo Film Co.Except for chemicals metioned above, 21896-59-3 is also used., Ltd., Japan). Ger. Offen. DE 4142960 A1 2 Jul 1992, 9 pp. (Germany). CODEN: GWXXBX. CLASS: ICM: C07C311-05. ICA: G03C005-30; G01N031-16. APPLICATION: DE 91-4142960 24 Dec 1991. PRIORITY: JP 90-405649 25 Dec 1990.In this experiment, several chemicals are used like 21896-59-3 DOCUMENT TYPE: Patent CA Section: 23 (Aliphatic Compounds) Section cross-reference(s): 54 Sulfonamide derivs. RSO2NHZ1NXY (R = alkyl, XZ2CO2M, WNZZ1HSO2R; Y = RSO2NHZ1, Z2CO2M; Z1, Z2 = alkylene; Z = Y; M = H, cation; X and Y are not simultaneously = Z2CO2M] were prepd. as metal chelators (no data). Thus, 0.42 mol ClCH2CH2NHSO2Me and 0.42 mol 5N NaOH were added to a soln. of 0.20 mol glycine in 0.20 mol 5N NaOH at 50°. The soln. was stirred 5 h at 50 to give (MeSO2NHCH2CH2)2NCH2CO2H in 32% yield. ..
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