Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.1411 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(N)=NC=C1
InChI
InChIKey=ORLGLBZRQYOWNA-UHFFFAOYSA-N
InChI=1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 2-Amino-4-methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo. | 1996 Nov |
|
| Rhodium(I)-catalyzed one-pot synthesis of dialkyl ketones from methanol and alkenes through directed sp3 C-H bond activation of N-methylamine. | 2008 Nov 30 |
|
| 2-Ferrocenyl-N-(2-ferrocenylbenzo-yl)-N-(4-methyl-2-pyrid-yl)benzamide. | 2009 Feb 28 |
|
| 4-Methyl-3-nitro-pyridin-2-amine. | 2009 Jun 20 |
|
| Robust recognition of malonate and 2-amino-4-picolinium in conjunction with M(II) as a triad (M = Ni/Co/Mn): role of this highly stable hydrogen-bonded motif in driving supramolecular self-assembly. | 2009 Oct 7 |
|
| Growth and characterization of 2-amino-4-picolinium 4-aminobenzoate single crystals. | 2010 Apr |
|
| Bis(2-amino-5-bromo-pyridinium) fumarate dihydrate. | 2010 Aug 11 |
|
| 2-Amino-4-methyl-pyridinium hexa-2,4-dienoate dihydrate. | 2010 Aug 25 |
|
| 2-Amino-4-methyl-pyridinium 4-nitro-benzoate. | 2010 Jan 13 |
|
| 2-Amino-4-methyl-pyridinium (E)-3-carb-oxy-prop-2-enoate. | 2010 Jul 10 |
|
| 2-Amino-4-methyl-pyridinium 3-carb-oxy-4-hy-droxy-benzene-sulfonate monohydrate. | 2010 Jul 24 |
|
| 2-Amino-4-methyl-pyridinium 2-hy-droxy-benzoate. | 2010 Jul 31 |
|
| 2-Amino-4-methylpyridinium 2-hy-droxy-3,5-dinitro-benzoate. | 2010 Jul 7 |
|
| 2-Amino-4-methyl-pyridinium 2-carb-oxy-benzoate. | 2010 Jul 7 |
|
| Bis(2-amino-4-methyl-pyridinium) terephthalate tetra-hydrate. | 2010 Jul 7 |
|
| Bis(2-amino-4-methyl-pyridinium) trans-diaqua-bis-(pyrazine-2,3-dicarboxyl-ato)cuprate(II) hexa-hydrate. | 2010 Jun 23 |
|
| 2-Amino-4-methyl-pyridinium 6-carb-oxy-pyridine-2-carboxyl-ate sesquihydrate. | 2010 Nov 20 |
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1490
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
394N1Z644H
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
176165
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
m1732
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | Merck Index | ||
|
172
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
695-34-1
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
1533
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
6972
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
DTXSID1044720
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY | |||
|
211-780-9
Created by
admin on Mon Mar 31 19:08:20 GMT 2025 , Edited by admin on Mon Mar 31 19:08:20 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD
