The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser.
For the best experience on our site, be sure to turn on Javascript in your browser.
This is a demo store. No orders will be fulfilled.
We use cookies to keep things working smoothly and to improve your experience.
Choose what’s okay for you below. See our Cookie Policy .
Accept Cookies
2-t-Butylamino-5-methyl-3-nitropyridine - 98%, high purity , CAS No.1033202-70-8
Discover 2-t-Butylamino-5-methyl-3-nitropyridine by Aladdin Scientific in 98% for only $1,631.90. Available - in Ligands at Aladdin Scientific. Tags: .
Basic Description
Synonyms
N-tert-butyl-5-methyl-3-nitropyridin-2-amine | MFCD10699717 | AKOS015838048 | A896509 | DTXSID90674456 | 2-T-BUTYLAMINO-5-METHYL-3-NITROPYRIDINE | BS-22953 | SB78678 | 1033202-70-8
Specifications & Purity
≥98%
Storage Temp
Room temperature
Shipped In
Normal
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic 1,3-dipolar compounds
Class
Allyl-type 1,3-dipolar organic compounds
Subclass
Organic nitro compounds
Intermediate Tree Nodes
C-nitro compounds
Direct Parent
Nitroaromatic compounds
Alternative Parents
Secondary alkylarylamines Methylpyridines Aminopyridines and derivatives Imidolactams Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Nitroaromatic compound - Aminopyridine - Methylpyridine - Secondary aliphatic/aromatic amine - Pyridine - Imidolactam - Heteroaromatic compound - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Secondary amine - Propargyl-type 1,3-dipolar organic compound - Amine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
N-tert-butyl-5-methyl-3-nitropyridin-2-amine
INCHI
InChI=1S/C10H15N3O2/c1-7-5-8(13(14)15)9(11-6-7)12-10(2,3)4/h5-6H,1-4H3,(H,11,12)
InChIKey
UUPQPXGBTGMRDO-UHFFFAOYSA-N
Smiles
CC1=CC(=C(N=C1)NC(C)(C)C)[N+](=O)[O-]
Isomeric SMILES
CC1=CC(=C(N=C1)NC(C)(C)C)[N+](=O)[O-]
PubChem CID
46738805
Molecular Weight
209.2
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Molecular Weight
209.240 g/mol
XLogP3
2.900
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
2
Exact Mass
209.116 Da
Monoisotopic Mass
209.116 Da
Topological Polar Surface Area
70.700 Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
232.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Solution Calculators
Molarity Calculator
Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator
Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator
Shall we send you a message when we have discounts available?
Remind me later
Allow
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
