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6304-29-6

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6304-29-6 Usage

Physical State

Yellow liquid

Odor

Strong, pungent

Common Uses

Production of fragrances and flavors
Pyridine-based chelating agent
Synthesis of pharmaceuticals

Research Areas

Potential as a metalloenzyme inhibitor
Investigated for treatment of human diseases such as cancer and neurodegenerative disorders

Check Digit Verification of cas no

The CAS Registry Mumber 6304-29-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6304-29:
(6*6)+(5*3)+(4*0)+(3*4)+(2*2)+(1*9)=76
76 % 10 = 6
So 6304-29-6 is a valid CAS Registry Number.

6304-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-pyridin-4-ylbutan-2-one

1.2 Other means of identification

Product number -
Other names -

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:6304-29-6 SDS

6304-29-6Downstream Products

6304-29-6Relevant articles and documents

Convenient Synthesis of 3-Methyl-1-(4-pyridinyl)-2-butanone using Phenyllithium as a Metalating Agent

Leon, P.,Garbay-Jaureguiberry, C.,Roques, B. P.

, p. 1547 - 1550 (2007/10/02)

3-Methyl-1-(4-pyridinyl)-2-butanone has been synthesized via a short and convenient method based upon acylation of 4-picoline by phenyllithium followed by reaction with ethyl isobutyrate.This procedure can be extendet to the preparation of various alkyl pyridyl ketones, intermediates in the synthesis of potential antitumor 6-substituted 7H-pyridocarbazole dimers.

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