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4810-79-1

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4810-79-1 Usage

General Description

4-Isobutyl-pyridine is an organic compound with the chemical formula C10H13N. It is a pyridine derivative with a branched isobutyl group attached to the nitrogen atom. 4-Isobutyl-pyridine has a strong odor and is commonly used as a flavoring ingredient in the food and beverage industry. It is also used as a fragrance ingredient in perfumes and personal care products. Additionally, 4-isobutyl-pyridine has been studied for its potential antimicrobial properties and has been found to have some insecticidal activity. It is important to handle this chemical with care, as it can be harmful if ingested or inhaled and may cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 4810-79-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4810-79:
(6*4)+(5*8)+(4*1)+(3*0)+(2*7)+(1*9)=91
91 % 10 = 1
So 4810-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N/c1-8(2)7-9-3-5-10-6-4-9/h3-6,8H,7H2,1-2H3

4810-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ISOBUTYL-PYRIDINE

1.2 Other means of identification

Product number -
Other names 4-Isobutylpyridin

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:4810-79-1 SDS

4810-79-1Relevant articles and documents

Efficient Diastereoselective Three-Component Synthesis of Pipecolic Amides

van der Heijden, Gydo,van Schaik, Timo B.,Mouarrawis, Valentinos,de Wit, Martin J. M.,Velde, Christophe M. L. Vande,Ruijter, Eelco,Orru, Romano V. A.

supporting information, p. 5313 - 5325 (2019/06/10)

An efficient Ugi-type three-component reaction (U-3CR) for the synthesis of pipecolic amides is reported. The U-3CR between electronically diverse isocyanides, carboxylic acids and 4-substituted Δ1-piperideines proceeds in a highly diastereoselective fashion. The Δ1-piperideines are obtained by NCS-mediated oxidation of the corresponding 4-substituted piperidines, which in turn are generated by an efficient two-step procedure involving the alkylation of 4-picoline and subsequent catalytic hydrogenation of the pyridine ring. We demonstrate the utility of this U-3CR, in combination with the convertible isocyanide 2-bromo-6-isocyanopyridine, in the synthesis of the anticoagulant argatroban.

Regioselective synthesis of 4-alkylpyridines from pyridine and aldehydes via dipole reversal process of 1,4-dihydropyridine phosphonate

Lee, Phil Ho,Lee, Kooyeon,Shim, Jun Hwan,Lee, Seong Guk,Kim, Sundae

, p. 777 - 784 (2007/10/03)

4-Alkylation of pyridine has been accomplished by the reaction of ylides, derivated from 1,4-dihydropyridine phosphonate via phosphonioalkoxycarbonylation of pyridine with aldehydes and subsequent elimination of diisopropyl phosphate followed by aromatization with potassium tert-butoxide.

LINCOMYCIN DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

-

Page 121-122, (2010/02/06)

Novel lincomycin derivatives are disclosed. These lincomycin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against bacteria, including gram positive organisms, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

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