ChemicalBook--->CAS DataBase List--->7521-41-7

7521-41-7

7521-41-7 Structure

7521-41-7 Structure
IdentificationMore
[Name]

2-Amino-3-pyridinecarboxaldehyde
[CAS]

7521-41-7
[Synonyms]

2-AMINO-3-FORMYLPYRIDINE
2-AMINO-3-PYRIDINECARBOXALDEHYDE
2-AMINONICOTINALDEHYDE
2-AMINO-PYRIDIN-3-CARBALDEHYDE
2-AMINO-PYRIDINE-3-CARBALDEHYDE
2-AMINOPYRIDINE-3-CARBOXALDEHYDE
3-PYRIDINECARBOXALDEHYDE, 2-AMINO-
2-Aminopyridine-3-carboxaldehyde, 2-Aminonicotinaldehyde
2-Amino-3-Pyridine Formaldehyde
2-Amino-3-formylpyridine, 2-Aminonicotinaldehyde
2-Aminopyridine-3-carboxaldehyde 99%
2-AMINO-3-PYRIDINECARBOXALDEHYDE 2-AMINONICOTINALDEHYDE
2-Aminopyridine-3-carboxyaldehyde
3-formylpyridin-2-amine
[EINECS(EC#)]

626-730-5
[Molecular Formula]

C6H6N2O
[MDL Number]

MFCD01830382
[Molecular Weight]

122.12
[MOL File]

7521-41-7.mol
Chemical PropertiesBack Directory
[Appearance]

yellow crystals
[Melting point ]

98-102 °C (lit.)
[Boiling point ]

290.7±25.0 °C(Predicted)
[density ]

1.264±0.06 g/cm3(Predicted)
[Fp ]

>300℃
[storage temp. ]

Refrigerator (+4°C)
[solubility ]

Soluble in Ether, Ethyl acetate, Chloroform (Slightly), Methanol (Slightly)
[form ]

Powder, Crystals and/or Chunks
[pka]

4.99±0.36(Predicted)
[color ]

Yellow to light brown
[Water Solubility ]

insoluble
[Sensitive ]

Air Sensitive
[Detection Methods]

HPLC
[BRN ]

109598
[InChI]

InChI=1S/C6H6N2O/c7-6-5(4-9)2-1-3-8-6/h1-4H,(H2,7,8)
[InChIKey]

NXMFJCRMSDRXLD-UHFFFAOYSA-N
[SMILES]

C1(N)=NC=CC=C1C=O
[CAS DataBase Reference]

7521-41-7(CAS DataBase Reference)
[Storage Precautions]

Air sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a-P261-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[PackingGroup ]

II
[HS Code ]

29339900
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

yellow crystals
[Uses]

2-Aminonicotinaldehyde is commonly employed as a starting material for a wide variety of N-heterocyclic compounds (e.g. β-nicotyrine [N445000]) . 2-Aminonicotinaldehyde is also used as a reagent to synthesize hydrazones (e.g.thionaphthenquinone 3-hydrazone [T367720]), which possess antituburcular properties.
[Preparation]

Preparative Methods of 2-Amino-3-pyridinecarboxaldehyde: the reagent is best when freshly prepared. A multistep procedure starting from 2-amino-3- picoline has been improved upon by a simple two-step approach. Sulfamation of nicotinamide with ammonium sulfamate (both commercially available) provides 2-(3′-pyridyl)pyrido[2,3-d]pyridimine which may be hydrolyzed in 2 N HCl to provide the reagent (eq 1)[1]. Substituted derivatives of the reagent may be prepared via a similar intermediate.
2-Amino-3-pyridinecarboxaldehyde synthesis
[Synthesis]

Pyrido[2,3-d]pyrimidine, 2-(3-pyridinyl)-

7521-27-9

2-Amino-3-pyridinecarboxaldehyde

7521-41-7

General procedure for the synthesis of 2-amino-3-pyridinecarboxaldehyde from the compound (CAS: 7521-27-9): first, a 2 mol/L hydrochloric acid solution was prepared. The dried feedstock was transferred to a 50 mL single neck flask and about 30 mL of the above hydrochloric acid solution was added. The mixture was heated to reflux for 4 hours and subsequently cooled to room temperature. The pH of the reaction mixture was adjusted to 7-8 using 10 mol/L sodium hydroxide solution. 5 extractions were carried out with ether and the organic phases were combined and dried over anhydrous potassium carbonate. The solvent was removed by rotary evaporation to give a yellow solid product. Finally, it was purified by column chromatography (unfolding agent ratio VD TM/VEIQH = 30:1) and dried at low temperature to obtain pure 2-amino-3-pyridinecarboxaldehyde in light yellow color in 30% yield.

[storage]

2-Amino-3-pyridinecarboxaldehyde is somewhat more stable than 2-Aminobenzaldehyde and may be stored for up to several months at 0 °C under an inert atmosphere. Sublimation is a convenient method for the separation of higher oligomers which may accumulate during storage. Use in a fume hood.
[References]

1. (a) Caluwe, P. T 1980, 36, 2359. (b) Cheng, C.-C.; Yan, S.-J. OR 1982, 28, 37. (c) Thummel, R. P. SL 1992, 1.
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-pyridinecarboxaldehyde(7521-41-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

2-Amino-3-pyridinecarboxaldehyde, 97%(7521-41-7)
[Alfa Aesar]

2-Aminopyridine-3-carboxaldehyde, 98%(7521-41-7)
[Sigma Aldrich]

7521-41-7(sigmaaldrich)
[TCI AMERICA]

2-Aminonicotinaldehyde,>97.0%(GC)(7521-41-7)
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