Sulfuryl chloride → HCID 178492872, compound
Reaction equation
[CH3:34][O:35][c:36]1[cH:37][c:38]([O:42][C:43]([F:44])([F:45])[F:46])[cH:39][cH:40][cH:41]1.[Cl:1][c:2]1[cH:3][c:4]2[c:8]([cH:9][cH:10]1)[NH:7][C:6](=[O:11])[C:5]2([c:12]1[c:13]([O:18][CH3:19])[cH:14][cH:15][cH:16][cH:17]1)[NH:20][CH:21]([C:22](=[O:23])[N:24]([CH3:25])[CH3:26])[CH2:27][OH:28].[S:29](=[O:30])(=[O:31])([Cl:32])[Cl:33]>>[Cl:1][c:2]1[cH:3][c:4]2[c:8]([cH:9][cH:10]1)[N:7]([S:29](=[O:30])(=[O:31])[c:39]1[c:38]([O:42][C:43]([F:44])([F:45])[F:46])[cH:37][c:36]([O:35][CH3:34])[cH:41][cH:40]1)[C:6](=[O:11])[C:5]2([c:12]1[c:13]([O:18][CH3:19])[cH:14][cH:15][cH:16][cH:17]1)[NH:20][CH:21]([C:22](=[O:23])[N:24]([CH3:25])[CH3:26])[CH2:27][OH:28]Participants
4
Sources & evidence
- ORD record
- ord-77d05d91121e4d1b832372d36603a0a6
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (5/10)
Reaction notes
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