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63053-27-0

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63053-27-0 Usage

Molecular weight

229.31 g/mol

Structure

2,4-pentanedione core with a 3-[[4-(dimethylamino)phenyl]methylene] group attached

Appearance

Yellow or pale yellow solid

Solubility

Soluble in organic solvents such as ethanol, acetone, and chloroform

Melting point

94-96°C

Boiling point

Not readily available due to its thermal instability

Functional groups

Carbonyl (C=O) and imine (N=C) groups are present in the molecule

Reactivity

Can undergo various organic reactions such as condensation, reduction, and cyclization

Chiral auxiliary potential

The compound has a chiral center in the dimethylamino-phenyl-methylene group, which can be used as a chiral auxiliary in organic synthesis.

Biological activities

The compound has been studied for its potential biological activities, but specific information is not available.

Flavoring agent

The compound may be used as a flavoring agent in the food industry, but specific applications are not mentioned.

Chemical intermediate

The compound can be used as a chemical intermediate in the production of other compounds, but specific examples are not provided.

Safety precautions

Handle with care and follow proper safety procedures to avoid potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 63053-27-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,5 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63053-27:
(7*6)+(6*3)+(5*0)+(4*5)+(3*3)+(2*2)+(1*7)=100
100 % 10 = 0
So 63053-27-0 is a valid CAS Registry Number.

63053-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[4-(dimethylamino)phenyl]methylidene]pentane-2,4-dione

1.2 Other means of identification

Product number -
Other names ms-(4-Dimethylamino-benzal)-acetylaceton

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:63053-27-0 SDS

63053-27-0Relevant articles and documents

A facile synthesis of trisubstituted alkenes from β-diketones and aldehydes with AlCl3 as catalyst

Li, Zheng-Nan,Chen, Xiao-Liang,Fu, Yu-Jie,Wang, Wei,Luo, Meng

experimental part, p. 25 - 35 (2012/05/20)

Preparation of trisubstituted alkenes from low-activity β-diketones and aldehydes with aluminum chloride as catalyst has been studied. The frequently used catalyst AlCl3 is used for the first time to promote this condensation. The procedure is a convenient, low toxicity, and highly efficient method for industrial synthesis of trisubstituted alkenes in high yield. Springer Science+Business Media B.V. 2011.

Concerning the identity test for caffeine in the pharmacopoeia: Part 2: Constitution of the dye from the modified reaction

Moehrle,Wirtz

, p. 269 - 279 (2007/10/03)

Under modified conditions the products of alkaline hydrolysis of caffeine and theophylline give blue dyes with imidazo[1,5-a-]pyrimidium salts as intermediates. From caffeidine results as final product - in contrary to the previous assumption the 2,4-bis-

Hydrolysis of Electrophilic Olefins. I. Kinetic Studies on the Hydrolysis of p-Dimethylaminobenzylidene Derivatives of Active Methylene Compounds.

Umeda, Tsuneji,Hirai, Eizo

, p. 2743 - 2752 (2007/10/02)

The dissociation constants (Ka) of the conjugate acids of the p-dimethylaminobenzylidene derivatives (I) of various active methylene compounds (XYCH2) were determined.Alkaline hydrolysis of I was studied kinetically in 30 percent (v/v) ethanol

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