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1122-71-0

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1122-71-0 Usage

Chemical Properties

Clear light brown liquid or low melting solid

Uses

Use as primary and secondary intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 1122-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1122-71:
(6*1)+(5*1)+(4*2)+(3*2)+(2*7)+(1*1)=40
40 % 10 = 0
So 1122-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO/c1-6-3-2-4-7(5-9)8-6/h2-4,9H,5H2,1H3

1122-71-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H26794)  6-Methyl-2-pyridinemethanol, 98%   

  • 1122-71-0

  • 1g

  • 216.0CNY

  • Detail
  • Alfa Aesar

  • (H26794)  6-Methyl-2-pyridinemethanol, 98%   

  • 1122-71-0

  • 5g

  • 710.0CNY

  • Detail
  • Alfa Aesar

  • (H26794)  6-Methyl-2-pyridinemethanol, 98%   

  • 1122-71-0

  • 25g

  • 2555.0CNY

  • Detail
  • Aldrich

  • (M78607)  6-Methyl-2-pyridinemethanol  98%

  • 1122-71-0

  • M78607-5G

  • 1,123.20CNY

  • Detail
  • Aldrich

  • (M78607)  6-Methyl-2-pyridinemethanol  98%

  • 1122-71-0

  • M78607-5G

  • 1,123.20CNY

  • Detail
  • Aldrich

  • (M78607)  6-Methyl-2-pyridinemethanol  98%

  • 1122-71-0

  • M78607-5G

  • 1,123.20CNY

  • Detail
  • Aldrich

  • (M78607)  6-Methyl-2-pyridinemethanol  98%

  • 1122-71-0

  • M78607-5G

  • 1,123.20CNY

  • Detail

1122-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Methyl-2-pyridinemethanol

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-6-methylpyridine

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:1122-71-0 SDS

1122-71-0Relevant articles and documents

SEQUENCE OF REPLACEMENT OF HYDROGEN IN 2,6-DIMETHYLPYRIDINE BY LITHIUM OR HALOGEN

Karpman, Ya.S.,Azimov, V.A.,Anisimova, O.S.,Yakhontov, L.N.

, p. 89 - 93 (1980)

It is shown that, according to the results of chromatographic mass spectrometry, the reaction of 2,6-dimethylpyridine with phenyllithium leads only to the monolithium derivative.The chlorination and bromination of 2,6-dimethylpyridine with various reagents were studied systematically.A method for the conversion of 2,6-bis(chloromethyl)pyridine to 2,6-bis(hydroxymethyl)pyridine is given.

-

Luz et al.

, p. 1114,1116 (1955)

-

IMPROVED PROCEDURES FOR PREPARATION OF 2-PYRIDONES AND 2-HYDROXYMETHYLPYRIDINES FROM PYRIDINE N-OXIDES

Konno, Katsuhiro,Hashimoto, Kimiko,Shirahama, Haruhisa,Matsumoto, Takeshi

, p. 2169 - 2172 (1986)

2-Pyridones and 2-hydroxymethylpyridines were prepared from pyridine N-oxides by treatment with trifluoroacetic anhydride in dimethylformamide.The reaction proceeds at room temperature in satisfactory yields.

-

Jones,Russell

, p. 2246 (1969)

-

Photochemical C-H Silylation and Hydroxymethylation of Pyridines and Related Structures: Synthetic Scope and Mechanisms

Rammal, Fatima,Gao, Di,Boujnah, Sondes,Hussein, Aqeel A.,Lalevée, Jacques,Gaumont, Annie-Claude,Morlet-Savary, Fabrice,Lakhdar, Sami

, p. 13710 - 13717 (2020/11/30)

Considering the synthetic relevance of heteroarenes in various areas ranging from organic synthesis to medicinal chemistry, developing practically simple methodologies to access functionalized heteroarenes is of a significant value. Described herein is an efficient approach for C-H silylation and hydroxymethylation of pyridines and related heterocycles by the combination of silanes or methanol with readily available N-methoxypyridinium ions with a low catalyst loading (2 mol %) under blue light irradiation. The synthetic importance of the developed reactions is demonstrated by the synthesis of biologically relevant compounds. Electron paramagnetic resonance spectroscopy, quantum yield measurements, and density-functional theory calculations allowed us to understand reaction mechanisms of both photocatalytic reactions.

ANALOGS OF 2-PRALIDOXIME AS ANTIDOTES AGAINST ORGANOPHOSPHORUS NERVE AGENTS

-

Paragraph 00120, (2020/02/23)

Provided herein are compounds useful in treating exposure to an organophosphorus compound, such as a nerve agent, pesticide, or, generally, an acetylcholinesterase inhibitor, such as sarin. Compositions, e.g. pharmaceutical compositions or dosage forms, comprising the compounds also are provided herein. Methods of treating a patient exposed to a nerve agent, pesticide, or, generally, an acetylcholinesterase inhibitor, e.g., an organophosphorus compound, such as sarin, also are provided.

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