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2-ACETOXY-1,3-BUTADIENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24454-89-5

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24454-89-5 Usage

Physical Properties

colorless liquid, sweet floral odor, highly flammable

Uses

production of pharmaceuticals, fragrances, building block for organic compounds

Health Risks

potential mutagen, respiratory irritant, should be avoided

Environmental Risks

potential risk for environmental contamination, precautions should be taken to prevent release into the environment

Check Digit Verification of cas no

The CAS Registry Mumber 24454-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24454-89:
(7*2)+(6*4)+(5*4)+(4*5)+(3*4)+(2*8)+(1*9)=115
115 % 10 = 5
So 24454-89-5 is a valid CAS Registry Number.

24454-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ACETOXY-1,3-BUTADIENE

1.2 Other means of identification

Product number -
Other names Glyceryl 2-acetate distearate

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:24454-89-5 SDS

24454-89-5Relevant academic research and scientific papers

Asymmetrie construction of rings A - D of Daphnicyclidin-type alkaloids

Dunn, Travis B.,Michael Ellis,Kofink, Christiane C.,Manning, James R.,Overman, Larry E.

supporting information; experimental part, p. 5658 - 5661 (2010/03/01)

[Chemical Equation Presented] The aza-Cope-Mannich reaction and ring-closing metathesis are key steps in the assembly of intermediates containing rings A - D of Daphniphyllum alkaloids of the daphnicyclidin type such as daphnipaxinin and oldhamine A.

Process for the preparation of unsaturated ketones

-

, (2008/06/13)

Ketones, which are intermediates in the synthesis of vitamin A or perfumes, and have the general formula: EQU1 wherein R1 is hydrogen or C1-10 hydrocarbon, R2 and R3 are hydrogen or C1-4 alkyl, R4 and R5 are hydrogen or together form a --CH2 --CH2 --C(CH3)2 -- group, R6 and R7 are hydrogen or C1-10 hydrocarbon, or together with the carbon atom to which they are joined form a hydrocarbon ring of up to 10 carbons, or EQU2 forms a hydrocarbon ring of up to 10 carbons joined through R6 and R8 or R7 and R8, R8 is hydrogen or C1-10 hydrocarbon and n is 0-6, are prepared by reacting an unsaturated halide of formula EQU3 wherein X is halogen, with an enol ester of formula EQU4 wherein R9 is C1-20 hydrocarbon, in the presence of a metal catalyst.

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