Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H7NO.ClH |
| Molecular Weight | 97.544 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CNOC
InChI
InChIKey=USZLCYNVCCDPLQ-UHFFFAOYSA-N
InChI=1S/C2H7NO.ClH/c1-3-4-2;/h3H,1-2H3;1H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Dialkylaluminum N,O-dimethylhydroxylamine complex as a reagent to mask reactive carbonyl groups in situ from nucleophiles. | 2010-12-03 |
|
| Direct one-pot synthesis of alpha-siloxy-Weinreb amides from aldehydes. | 2007-12-07 |
|
| 2-acetamido-N-benzyl-2-(methoxyamino)acetamides: functionalized amino acid anticonvulsants. | 2005-07 |
|
| A convenient method for the conversion of hindered carboxylic acids to N-methoxy-N-methyl (Weinreb) amides. | 2004-12-10 |
|
| Preparation of Weinreb amides using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). | 2004-04 |
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6638-79-5
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DTXSID3064433
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73200
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48292
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229-642-1
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3PN4EY7H9S
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admin on Tue Apr 01 18:48:38 GMT 2025 , Edited by admin on Tue Apr 01 18:48:38 GMT 2025
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD