Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H10ClN |
| Molecular Weight | 107.582 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)CCCl
InChI
InChIKey=WQMAANNAZKNUDL-UHFFFAOYSA-N
InChI=1S/C4H10ClN/c1-6(2)4-3-5/h3-4H2,1-2H3
| Molecular Formula | C4H10ClN |
| Molecular Weight | 107.582 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Novel tricyclic pyrazole BRAF inhibitors with imidazole or furan central scaffolds. | 2010-09-15 |
|
| The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate. | 2009-12-04 |
|
| Investigation of trypanothione reductase as a drug target in Trypanosoma brucei. | 2009-12 |
|
| Synthesis of surfactants based on pentaerythritol. I. Cationic and zwitterionic gemini surfactants. | 2009-10-16 |
|
| Enhanced electron transfer dissociation through fixed charge derivatization of cysteines. | 2009-10-01 |
|
| Genome-wide requirements for resistance to functionally distinct DNA-damaging agents. | 2005-08 |
|
| [Tetracyclic derivatives of diltiazem from aurones and thioaurones]. | 2003-03 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:43:55 GMT 2025
by
admin
on
Mon Mar 31 18:43:55 GMT 2025
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| Record UNII |
9UK81G2OHJ
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| Record Status |
Validated (UNII)
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| Record Version |
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DTXSID2059356
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9UK81G2OHJ
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107-99-3
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7901
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123444
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1917
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78155
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C114993
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203-540-7
Created by
admin on Mon Mar 31 18:43:55 GMT 2025 , Edited by admin on Mon Mar 31 18:43:55 GMT 2025
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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