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13562-84-0

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13562-84-0 Usage

General Description

ACETOACETIC ACID HEXYL ESTER is a chemical compound often used in the production of various items like paints, inks, and other similar products. This organic compound falls into the ester group of chemicals, which are known for their distinct, often fruity smells. ACETOACETIC ACID HEXYL ESTER can also be found in perfumes and other fragrance products. The compound is known by some alternative names like Hexyl 3-oxobutanoate and Hexyl acetoacetate. While mostly safe, it can cause irritation upon skin contact or if it's ingested or inhaled, requiring safety measures during its handling and usage.

Check Digit Verification of cas no

The CAS Registry Mumber 13562-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13562-84:
(7*1)+(6*3)+(5*5)+(4*6)+(3*2)+(2*8)+(1*4)=100
100 % 10 = 0
So 13562-84-0 is a valid CAS Registry Number.

13562-84-0 Well-known Company Product Price

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  • TCI America

  • (A0913)  Hexyl Acetoacetate  >97.0%(GC)

  • 13562-84-0

  • 25mL

  • 790.00CNY

  • Detail

13562-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Hexyl Acetoacetate

1.2 Other means of identification

Product number -
Other names Acetoacetic Acid Hexyl Ester

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:13562-84-0 SDS

13562-84-0Relevant articles and documents

Combined experimental and computational studies of heterobimetallic Bi-Rh paddlewheel carboxylates as catalysts for metal carbenoid transformations

Hansen, Jorn,Li, Bo,Dikarev, Evgeny,Autschbach, Jochen,Davies, Huw M. L.

, p. 6564 - 6571 (2009)

(Chemical Equation Presented) The catalytic activity of heterobimetallic Bi-Rh paddlewheel carboxylate complexes has been evaluated for the first time in the context of metal carbenoid chemistry. The Bi-Rh carboxylate complexes were found to effectively catalyze both cyclopropanation reactions and C-H insertions as well as reactions involving ylide intermediates with similar selectivity profiles to analogous dirhodium complexes. The heterometallic complex BiRh(O2CCF3)3(O2CCH3) was found to be approximately 1600 times less reactive than its homometallic analogue Rh2(O2CCF3)3(O 2CCH3) toward the decomposition of methyl phenyldiazoacetate. The observed difference in reactivity is in good agreement with a computational model system where axial coordination to the second rhodium active site is considered for the dirhodium catalyst.

Ag-Cu nanoparticles as efficient catalysts for transesterification of β-keto esters under acid/base-free conditions

Yue, Hongmei,Yu, Hao,Liu, Sheng,Xu, Chunli

, p. 19041 - 19051 (2016/03/01)

Transesterification of β-keto esters and alcohols are traditionally catalyzed by acid or basic catalysts. However, these traditional catalysts do not always meet the requirements of modern synthetic chemistry which need to be highly efficient, selective, and environmentally friendly. In this work, Ag-Cu metal sites were first introduced as transesterification catalysts. The effect of the support, Ag:Cu molar ratio, and reaction conditions were investigated. The Ag-Cu metal sites were proved to be active in the β-ketoester transesterification with various alcohols, having yields comparable to the conventional acid- or base-catalysts.

Nano CuFe2O4: An efficient, magnetically separable catalyst for transesterification of β-ketoesters

Gohain, Mukut,Kumar, Vinod,Van Tonder, Johannes H.,Swart, Hendrik C.,Ntwaeaborwa, Odireleng M.,Bezuidenhoudt, Barend C. B.

, p. 18972 - 18976 (2015/03/04)

The preparation of a variety of β-ketoesters was achieved in high yields from methyl acetoacetate under neutral conditions through the utilization of magnetic CuFe2O4 nanoparticles as catalyst. Recycling of the catalyst was performed up to eight times without significant loss in activity. The catalyst was characterized using XRD, XPS, SEM and TEM techniques.

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