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4-METHYLNICOTINALDEHYDE is a chemical compound that serves as an important intermediate in the synthesis of pharmaceutical drugs due to its aldehyde derivative nature of nicotine. It is also utilized as a flavor and fragrance ingredient in consumer products, and has potential applications in the field of organic chemistry for developing new chemical reactions and synthetic methods. Its unique chemical structure and properties make it a valuable and versatile compound in various industrial and research applications.

51227-28-2

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51227-28-2 Usage

Uses

Used in Pharmaceutical Industry:
4-METHYLNICOTINALDEHYDE is used as a key intermediate in the synthesis of various pharmaceutical drugs, contributing to the development of new medications and therapies.
Used in Flavor and Fragrance Industry:
4-METHYLNICOTINALDEHYDE is used as a flavor and fragrance ingredient in consumer products such as perfumes and food items, enhancing their sensory appeal.
Used in Organic Chemistry Research:
4-METHYLNICOTINALDEHYDE is used in the field of organic chemistry for the development of new chemical reactions and synthetic methods, advancing scientific knowledge and innovation in chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 51227-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51227-28:
(7*5)+(6*1)+(5*2)+(4*2)+(3*7)+(2*2)+(1*8)=92
92 % 10 = 2
So 51227-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO/c1-6-2-3-8-4-7(6)5-9/h2-5H,1H3

51227-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylpyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-methyl-3-pyridinecarboxylate

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:51227-28-2 SDS

51227-28-2Relevant articles and documents

Synthesis of amphikuemin and analogs: a synomone that mediates partner-recognition between anemonefish and sea anemone

Konno, Katsuhiro,Qin, Guo-wei,Nakanishi, Koji

, p. 247 - 251 (2007/10/02)

Amphikuemin (1), a compound that is responsible for partner-recognition at the first encounter between anemonefish and sea anemones, has been synthesized to confirm its structure and to supply material for further biological studies.Synthesis of amphikuemin analogs (11-15) is also described.

REACTIVITY OF METHYL DERIVATIVES OF NITROGENOUS HETEROCYCLES IN VAPOR-PHASE CATALYTIC OXIDATION

Leitis, L. Ya.,Skolmeistere, R. A.,Golender, L. O.,Yansone, D. P.,Meksh, P. A.,Shimanskaya, M. V.

, p. 63 - 66 (2007/10/02)

A study has been made of the reactivity of methylpyridines, methylpyrazines, and methylquinolines in oxidation in the vapor phase in the presence of β-VO(PO3)2.Relationships have been found between the overall reaction rates of heterocyclic compounds and the charge on the ring nitrogen, and between the partial oxidation rate and the charge on the ring carbon atom adjacent to the methyl group.The partial oxidation rate of methylpyridines is given to a first approximation by the Hammett-type expression lnWa = -3.5 + 4.6 Σ?, with a correlation coefficient of 0.93.

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