Molecule:100509: Difference between revisions
From ChemWiki
molecule
(auto-generated) Tags: Manual revert Reverted |
(auto-generated) Tags: Manual revert Reverted |
||
Line 11: | Line 11: | ||
|moleculeKey=CMNUYDSETOTBDE-UHFFFAOYSA-N | |moleculeKey=CMNUYDSETOTBDE-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn= | ||
-INDIGO- | -INDIGO-07072219412D | ||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
Line 17: | Line 17: | ||
M V30 COUNTS 16 17 0 0 0 | M V30 COUNTS 16 17 0 0 0 | ||
M V30 BEGIN ATOM | M V30 BEGIN ATOM | ||
M V30 1 | M V30 1 N 4.75 -5.57501 0.0 0 | ||
M V30 2 C | M V30 2 C 3.88399 -5.07501 0.0 0 | ||
M V30 3 C | M V30 3 C 3.88399 -4.07499 0.0 0 | ||
M V30 4 C | M V30 4 C 4.75 -3.57499 0.0 0 | ||
M V30 5 C | M V30 5 C 5.61601 -4.07499 0.0 0 | ||
M V30 6 C 5. | M V30 6 C 5.61601 -5.07501 0.0 0 | ||
M V30 7 | M V30 7 C 4.75 -6.57501 0.0 0 | ||
M V30 8 C | M V30 8 C 5.61603 -7.07501 0.0 0 | ||
M V30 9 | M V30 9 C 6.48205 -6.57503 0.0 0 | ||
M V30 10 | M V30 10 C 7.34809 -7.07504 0.0 0 | ||
M V30 11 C | M V30 11 C 7.3481 -8.07503 0.0 0 | ||
M V30 12 C | M V30 12 C 6.48208 -8.57502 0.0 0 | ||
M V30 13 C | M V30 13 C 5.61604 -8.07501 0.0 0 | ||
M V30 14 C | M V30 14 C 6.48204 -3.575 0.0 0 | ||
M V30 15 | M V30 15 N 7.34806 -4.075 0.0 0 | ||
M V30 16 | M V30 16 O 6.48204 -2.575 0.0 0 | ||
M V30 END ATOM | M V30 END ATOM | ||
M V30 BEGIN BOND | M V30 BEGIN BOND | ||
M V30 1 1 | M V30 1 1 1 2 | ||
M V30 2 2 | M V30 2 2 2 3 | ||
M V30 3 | M V30 3 1 3 4 | ||
M V30 4 1 | M V30 4 1 4 5 | ||
M V30 5 | M V30 5 2 5 6 | ||
M V30 6 1 | M V30 6 1 6 1 | ||
M V30 7 1 7 | M V30 7 1 1 7 | ||
M V30 8 1 | M V30 8 1 7 8 | ||
M V30 9 | M V30 9 1 8 9 | ||
M V30 10 | M V30 10 2 9 10 | ||
M V30 11 1 | M V30 11 1 10 11 | ||
M V30 12 2 | M V30 12 2 11 12 | ||
M V30 13 | M V30 13 1 12 13 | ||
M V30 14 | M V30 14 2 13 8 | ||
M V30 15 1 | M V30 15 1 5 14 | ||
M V30 16 | M V30 16 1 14 15 | ||
M V30 17 | M V30 17 2 14 16 | ||
M V30 END BOND | M V30 END BOND | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
|smiles= | |smiles=N(CC1=CC=CC=C1)1C=C(C(=O)N)CC=C1 | ||
|inchi=1S/C13H14N2O/c14-13(16)12-7-4-8-15(10-12)9-11-5-2-1-3-6-11/h1-6,8,10H,7,9H2,(H2,14,16) | |inchi=1S/C13H14N2O/c14-13(16)12-7-4-8-15(10-12)9-11-5-2-1-3-6-11/h1-6,8,10H,7,9H2,(H2,14,16) | ||
|inchikey=CMNUYDSETOTBDE-UHFFFAOYSA-N | |inchikey=CMNUYDSETOTBDE-UHFFFAOYSA-N | ||
|width=300px | |width=300px | ||
|height=200px | |height=200px | ||
|float= | |float=left | ||
|logP= | |logP= | ||
|parent= | |parent= | ||
}} | }} |
Revision as of 16:44, 4 January 2024
Properties | |
---|---|
CID | 95276 |
CAS | 952-92-1 |
IUPAC-Name | 1-(phenylmethyl)-4h-pyridine-3-carboxamide |
Abbreviation | BNAH |
Trivialname | 1-benzyl-14-dihydronicotinamide |
Exact mass | 214.110613074 |
Molecular formula | C13H14N2O |
LogP | n/a |
Has vendors | true |
Molecular role | n/a |
Synonyms | 1-benzyl-14-dihydronicotinamide,benzyldihydronicotinamide,1-benzyl-14-dihydropyridine-3-carboxamide,1-benzyl-4h-pyridine-3-carboxamide,bnah,3-pyridinecarboxamide 14-dihydro-1-(phenylmethyl)-,hsu8ja8rmp,unii-hsu8ja8rmp,14-dihydro-n-1-benzylnicotinamide,nsc-26899 |
Click here to copy MOL-file.
Click here to show SMILES and InChI.
Molecule is used on following pages
topic
- Photocatalytic CO2 conversion to CO
- Homogeneous photocatalytic CO2 conversion
- Photocatalytic CO2 conversion to HCOOH
publication
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3
- Photocatalytic CO2 reduction using a Mn complex as a catalyst
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH
investigation
- Mn-carbonyl molecular catalysts containing a redox-active phenanthroline-5,6-dione for selective electro- and photoreduction of CO2 to CO or HCOOH/Table 1
- Photocatalytic CO2 reduction using a Mn complex as a catalyst/Photocatalytic CO2 reduction: conditions optimization
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 1
- Photocatalytic Reduction of Carbon Dioxide to CO and HCO2H Using fac-Mn(CN)(bpy)(CO)3/Table 2
other
Molecule roles
Investigation type | Electron donor |
---|---|
Photocatalytic CO2 conversion experiments | |
Cyclic Voltammetry experiments |