Sulfuryl chloride → HCID 67428844, compound
Reaction equation
[CH3:35][O:36][c:37]1[cH:38][c:39]([O:43][C:44]([F:45])([F:46])[F:47])[cH:40][cH:41][cH:42]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][CH2:21][CH2:22][C:23](=[O:24])[O:25][C:26]([CH3:27])([CH3:28])[CH3:29].[S:30](=[O:31])(=[O:32])([Cl:33])[Cl:34]>>[Cl:1][c:2]1[cH:3][c:4]2[c:8]([cH:9][cH:10]1)[N:7]([S:30](=[O:31])(=[O:32])[c:40]1[c:39]([O:43][C:44]([F:45])([F:46])[F:47])[cH:38][c:37]([O:36][CH3:35])[cH:42][cH:41]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][CH2:21][CH2:22][C:23](=[O:24])[O:25][C:26]([CH3:27])([CH3:28])[CH3:29]Participants
4
Sources & evidence
- ORD record
- ord-1139fcf629fb49feb1889e416f68763f
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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