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6-Acetylpyridine-2-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122637-39-2 Structure
  • Basic information

    1. Product Name: 6-Acetylpyridine-2-carboxylic acid
    2. Synonyms: 6-Acetylpyridine-2-carboxylic acid;2-Pyridinecarboxylic acid, 6-acetyl- (9CI);6-ACETYLPICOLINIC ACID;6-Acetyl-2-pyridinecarboxylic acid;6-acetylpyridin-2-carboxylic acid;2-Pyridinecarboxylic acid, 6-acetyl-
    3. CAS NO:122637-39-2
    4. Molecular Formula: C8H7NO3
    5. Molecular Weight: 165.14608
    6. EINECS: N/A
    7. Product Categories: GLYCINESCAFFOLD;ACETYLGROUP
    8. Mol File: 122637-39-2.mol
  • Chemical Properties

    1. Melting Point: 137℃
    2. Boiling Point: 360.4 °C at 760 mmHg
    3. Flash Point: 171.8 °C
    4. Appearance: /
    5. Density: 1.303 g/cm3
    6. Vapor Pressure: 8.01E-06mmHg at 25°C
    7. Refractive Index: 1.565
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 0.65±0.50(Predicted)
    11. Water Solubility: Slightly soluble in water.
    12. CAS DataBase Reference: 6-Acetylpyridine-2-carboxylic acid(CAS DataBase Reference)
    13. NIST Chemistry Reference: 6-Acetylpyridine-2-carboxylic acid(122637-39-2)
    14. EPA Substance Registry System: 6-Acetylpyridine-2-carboxylic acid(122637-39-2)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 122637-39-2(Hazardous Substances Data)

122637-39-2 Usage

Uses

Used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 122637-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122637-39:
(8*1)+(7*2)+(6*2)+(5*6)+(4*3)+(3*7)+(2*3)+(1*9)=112
112 % 10 = 2
So 122637-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO3/c1-5(10)6-3-2-4-7(9-6)8(11)12/h2-4H,1H3,(H,11,12)

122637-39-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H34059)  6-Acetylpyridine-2-carboxylic acid, 95%   

  • 122637-39-2

  • 250mg

  • 1159.0CNY

  • Detail
  • Alfa Aesar

  • (H34059)  6-Acetylpyridine-2-carboxylic acid, 95%   

  • 122637-39-2

  • 1g

  • 3217.0CNY

  • Detail

122637-39-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Acetylpyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylicacid,6-acetyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122637-39-2 SDS

122637-39-2Relevant articles and documents

Copper(ii)-hydroxide facilitated C-C bond formation: The carboxamido pyridine system: Versus the methylimino pyridine system

Fan, Weibin,Huang, Deguang,Li, Yinghua,Xiang, Shiqun,Xie, Xingkun,Zhang, Zilong

, p. 12189 - 12196 (2020/10/02)

A copper(ii)-hydroxide-induced carbon-carbon bond formation reaction is explored with the synthesis of an asymmetric carboxamido-methylimino pyridine Cu(i) complex of [CuI(py(N-CO)(NC-C)ph2Me2)2]- (12). Two imine-methyl groups are coupled to form a bridge

NEAR-INFRARED-RAY-ABSORBING COMPOSITION, NEAR-INFRARED-RAY CUT FILTER USING SAME, MANUFACTURING METHOD THEREFOR, CAMERA MODULE, AND MANUFACTURING METHOD THEREFOR

-

Paragraph 0852; 0854; 0855, (2017/01/02)

Provided are a near-infrared-ray-absorbing composition having strong near-infrared shielding properties when a cured film is produced, a near-infrared-ray cut filter, a manufacturing method therefor, a camera module, and a manufacturing method therefor. The near-infrared-ray-absorbing composition includes a copper complex obtained by reacting a compound (A) having at least two coordination sites with a copper component.

Linkage isomerism in transition-metal complexes of mixed (arylcarboxamido)(arylimino)pyridine ligands

Boyce, David W.,Salmon, Debra J.,Tolman, William B.

, p. 5788 - 5796 (2014/06/23)

The synthesis of a series of asymmetric mixed 2,6-disubstituted (arylcarboxamido)(arylimino)pyridine ligands and their coordination chemistry toward a series of divalent first-row transition metals (Cu, Co, and Zn) have been explored. Complexes featuring both anionic N,N,N″-carboxamido and neutral O,N,N-carboxamide coordination have been prepared and characterized by X-ray crystallography, cyclic voltammetry, and UV-visible and EPR spectroscopy. Specifically, RLM(X) (M = Cu; X = Cl-, OAc-) and RL(H)MX2 (M = Cu, Co, Zn; X = Cl-, SbF 6-) complexes that feature N,N,N″- or O,N,N-coordination are presented. Base-induced linkage isomerization from O,N,N-carboxamide to N,N,N″-carboxamido coordination is also confirmed by multiple forms of spectroscopy.

Microwave-promoted syntheses of pyridine carboxamides and tert-carboximides from novel 6-acetylpyridine-2-carboxylic acid

Su, Biyun,Zhao, Jianshe,Zhang, Qunzheng,Qin, Wenlong

experimental part, p. 4429 - 4440 (2010/05/01)

A novel 6-acetylpyridine-2-carboxylic acid (4) was obtained occasionally during the synthesis of asymmetric ethyl 6-acetylpyridine-2-carboxylate (3) from 2,6-dipiclinic acid (1). Compounds 3 and 4 could transform mutually under some specific conditions. T

Polynuclear lanthanide complexes of a series of bridging ligands containing two tridentate N,N′,O-donor units: Structures and luminescence properties

Ronson, Tanya K.,Adams, Harry,Harding, Lindsay P.,Pope, Simon J. A.,Sykes, Daniel,Faulkner, Stephen,Ward, Michael D.

, p. 1006 - 1022 (2007/10/03)

A set of three potentially bridging ligands containing two tridentate chelating N,N′,O-donor (pyrazole-pyridine-amide) donors separated by an o, m, or p-phenylene spacer has been prepared and their coordination chemistry with lanthanide(iii) ions investig

Further Pyridine Derivatives Isolated from the Culture Medium of Pseudomonas putida - Genuine Metabolites or Artefacts?

Budzikiewicz, H.,Hildebrand, U.,Ockels, W.,Reiche, M.,Taraz, K.

, p. 516 - 520 (2007/10/02)

From the culture medium of Pseudomonas putida after treatment with CH2N2 besides the expected Pyridine-2,6-di(monothiocarboxylic acid)-di-S-methyl ester a series of pyridine derivatives could be isolated which could be shown to be artefacts formed from pyridine-2,6-di(monothiocarboxylic acid). - Keywords: Pyridine Derivatives, Bacterical Metabolites, Pseudomonas putida, Thiocarboxylic Acid Chemistry

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