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1132-86-1

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1132-86-1 Usage

Type of Compound

Ester

Common Uses

Synthesis of pharmaceuticals and organic compounds
Flavoring agent in the food industry
Fragrance ingredient in cosmetic products

Odor

Pleasant fruity

Potential Therapeutic Properties

Anti-inflammatory effects
Antinociceptive effects

Applications

Pharmaceutical industry (medication development)
Food industry (flavoring)
Cosmetic industry (fragrance)

Scientific Research and Development

Valuable compound for research due to its diverse applications and potential therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1132-86-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1132-86:
(6*1)+(5*1)+(4*3)+(3*2)+(2*8)+(1*6)=51
51 % 10 = 1
So 1132-86-1 is a valid CAS Registry Number.

1132-86-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-acetylcyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Acetyl-cyclohexancarbonsaeure-aethylester

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:1132-86-1 SDS

1132-86-1Relevant articles and documents

Ion Pairing and Reactivity of the Alkali-Metal and Alkaline-Earth-Metal Derivatives of Ethyl (5-Bromopentyl)acetoacetate

Cacciapaglia, Roberta,Mandolini, Luigi

, p. 2579 - 2582 (1988)

The effect added alkali-metal and alkaline-earth-metal salts on the rate of intramolecular alkylation of the title compound has been investigated in 99percent aqueous Me2SO.It was found that the rate is practically insensitive to Et4N+ and K+ ions and it is slightly decreased by Na+ ion, but it is strongly depressed by Li+, Ba2+, Sr2+, Ca2+, and Mg2+ ions, the observed effects ranging over nearly 5 powers of ten.Analysis of rate data was carried out by means of a self-consistent approach, as based on the classical Acree hypothesis of independent contributions of free ions and ion pairs to the overall rate.In most cases it was possible to measure the ion pairing association constants (Kip) together with specific rates for reactions of the ion pairs (kip), even when the latter are much lower than the specific rate for reaction of the free ion (ki).The results show that ion pairing decreases in the order Li > Na > K and Mg > Ca > Sr > Ba, which clearly suggests that association is dominated by coulombic interactions.The strong inhibition caused by ion pairing is due to a greater cation interaction with the anionic reactant than with the transition state, where a significant fraction of the available negative charge is concentrated in the C-C bond-forming region.

Perkin-Markovnikov type reaction initiated with electrogenerated superoxide ion

Ojima,Osa

, p. 3187 - 3194 (2007/10/02)

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The total synthesis of (±)-trichostatin A. Some observations on the acylation and alkylation of silyl enol ethers, silyl dienol ethers and a silyl trienol ether

Fleming,Iqbal,Krebs

, p. 841 - 846 (2007/10/02)

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