Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H9NO2 |
| Molecular Weight | 103.1198 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCON=O
InChI
InChIKey=JQJPBYFTQAANLE-UHFFFAOYSA-N
InChI=1S/C4H9NO2/c1-2-3-4-7-5-6/h2-4H2,1H3
| Molecular Formula | C4H9NO2 |
| Molecular Weight | 103.1198 |
| 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 |
|---|---|---|
| Chemoselective nitration of phenols with tert-butyl nitrite in solution and on solid support. | 2009-09-17 |
|
| Photolysis of n-butyl nitrite and isoamyl nitrite at 355 nm: a time-resolved Fourier transform infrared emission spectroscopy and ab initio study. | 2009-05-07 |
|
| Photodissociation dynamics of alkyl nitrites at 266 and 355 nm: the OH product channel. | 2009-04-09 |
|
| O,O'-Diethyl {(Z)-[(2-chloro-phen-yl)(cyano)methyl-ene]amino-oxy}thio-phospho-nate. | 2009-03-06 |
|
| Vibrational analysis of n-butyl, isobutyl, sec-butyl and tert-butyl nitrite. | 2007-05 |
|
| Synthesis of peroxynitrite using isoamyl nitrite and hydrogen peroxide in a homogeneous solvent system. | 2006-07-15 |
|
| Aphrodisiac drug-induced hemolysis. | 2004 |
|
| Synthesis of N-substituted N-nitrosohydroxylamines as inhibitors of mushroom tyrosinase. | 2001-05 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:59:48 GMT 2025
by
admin
on
Mon Mar 31 17:59:48 GMT 2025
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| Record UNII |
44P8QG0F3T
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| Record Status |
Validated (UNII)
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| Record Version |
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| Code System | Code | Type | Description | ||
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208-862-1
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m2855
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PRIMARY | Merck Index | ||
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44P8QG0F3T
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Butyl nitrite
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C024225
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544-16-1
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8426
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10996
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DTXSID8049418
Created by
admin on Mon Mar 31 17:59:48 GMT 2025 , Edited by admin on Mon Mar 31 17:59:48 GMT 2025
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