Palmitoyl chloride → HCID 178450352, compound

HRID 2334079Notes

Reaction equation

HRID 2334079 reaction equation
[C:1]([CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])(=[O:17])[C:18]1([n:26]2[cH:27][n:28][c:29]3[c:30](=[O:31])[nH:32][c:33]([NH2:34])[n:35][c:36]23)[CH2:19][CH:20]([OH:21])[CH:22]([CH2:23][OH:24])[O:25]1.[C:37]([Cl:38])(=[O:39])[CH2:40][CH2:41][CH3:42].[C:43]([Cl:44])(=[O:45])[CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH2:58][CH2:59][CH3:60]>>[C:1]([CH2:2][CH2:3][CH3:4])(=[O:17])[C:18]1([n:26]2[cH:27][n:28][c:29]3[c:30](=[O:31])[nH:32][c:33]([NH2:34])[n:35][c:36]23)[CH2:19][CH:20]([OH:21])[CH:22]([CH2:23][OH:24])[O:25]1

Participants

4

Reactant 3

HCID 8206Palmitoyl chlorideHCID 8855Butyryl chlorideHCID 178443056HCID 178443056, compound

Product 1

HCID 178450352HCID 178450352, compound

Sources & evidence

ORD record
ord-d32bf4b4a6bc450582ee4b1051973132
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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