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2200-53-5

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2200-53-5 Usage

Physical state

Colorless liquid
Clear and transparent appearance

Odor

Pungent
Strong and irritating smell

Classification

Ketone
A carbonyl group (C=O) is bonded to an alkyl group (hydrocarbon chain)

Uses

Synthetic intermediate
Commonly used in the production of pharmaceuticals, fragrances, and other organic compounds

Key building block

Polymers and resins
Important component in the synthesis of various types of polymers and resins

Reactivity

High
Due to the presence of a carbonyl group and a vinyl group, it is highly reactive

Handling precautions

Risks to human health and environment
Proper management and handling are necessary to minimize potential hazards

Proper storage and disposal

Essential
To prevent accidents and environmental contamination, 1,2-Pentadiene-4-one should be stored and disposed of according to safety guidelines and regulations

Check Digit Verification of cas no

The CAS Registry Mumber 2200-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2200-53:
(6*2)+(5*2)+(4*0)+(3*0)+(2*5)+(1*3)=35
35 % 10 = 5
So 2200-53-5 is a valid CAS Registry Number.

2200-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name penta-3,4-dien-2-one

1.2 Other means of identification

Product number -
Other names 3,4-Pentadien-2-one

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:2200-53-5 SDS

2200-53-5Relevant articles and documents

VINYL ESTERS OF PHOSPHORUS ACIDS. XXVII. CHEMICAL PROPERTIES OF O-PHOSPHORYLATED ALDEHYDES AND KETONES

Kim, T. V.,Kiseleva, E. I.,Struchkov, Yu. T.,Antipin, M. Yu.,Chernega, A. N.,Gololobov, Yu. G.

, p. 2220 - 2235 (2007/10/02)

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PHOTOCHEMICAL CYCLOADDITION OF α,β-ACETYLENIC KETONES WITH SIMPLE OLEFINS

Hussain, Saadat,Agosta, William C.

, p. 3301 - 3306 (2007/10/02)

Irradiation of 3-pentyn-2-one (1) in the presence of tetramethylethylene, isobutylene, and cis- and trans-2-butene leads to vinyldihydrofurans 3, 5, 6, 8, and 9 (Table 1) in a novel photochemical cycloaddition reaction.A related adduct 13 is formed between tetramethylethylene and 5,5-dimethyl-3-hexyn-2-one (2).A mechanism incorporating an initial biradical that closes to a carbene (eqn 3) is proposed to account for these reactions.

VINYL CATIONS 33: 1-ALKENE-3-YNE-2-YL TRIFLATES, PRECURSORS OF TRIPLE BOND STABILIZED VINYL CATIONS-SYNTHESIS AND FIRST SOLVOLYTIC STUDIES.

Hassdenteufel, Juergen Rolf,Hanack, Michael

, p. 503 - 506 (2007/10/02)

The α-alkynyl vinyl triflates (3) are synthesized and the solvolyses reactions studied in different solvents.The solvolysis products and kinetic data indicate, that the hitherto unknown triple bond stabilized vinyl cation 2a 2b is formed as an intermediate.

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