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1126-41-6

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1126-41-6 Usage

General Description

"(1R)-(-)-Neoisocarvomenthol" is a chemical compound that belongs to the class of monoterpenoid alcohols. It is a stereoisomer of neoisocarvomenthol, meaning it has the same molecular formula and connectivity of atoms but a different arrangement of atoms in space. (1R)-(-)-Neoisocarvomenthol is commonly found in essential oils, particularly in the oils of certain plants such as Mentha species, and is responsible for the characteristic minty, cooling aroma and flavor. It is used in various industries, including the food and beverage industry for flavoring and aroma, as well as in pharmaceuticals and cosmetics for its cooling and soothing properties. Additionally, it has shown potential for use as an antimicrobial agent and in insecticidal and repellent products.

Check Digit Verification of cas no

The CAS Registry Mumber 1126-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1126-41:
(6*1)+(5*1)+(4*2)+(3*6)+(2*4)+(1*1)=46
46 % 10 = 6
So 1126-41-6 is a valid CAS Registry Number.

1126-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-isopropyl-2-methylcyclohexanol

1.2 Other means of identification

Product number -
Other names Cyclohexanol, 2-methyl-5-(1-methylethyl)-, [1S-(1α,2α,5α)]-

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:1126-41-6 SDS

1126-41-6Relevant articles and documents

Simple H2-free hydrogenation of unsaturated monoterpenoids catalyzed by Raney nickel

Philippov, Alexey A.,Chibiryaev, Andrey M.,Martyanov, Oleg N.

, p. 380 - 381 (2019/08/20)

A series of monoterpenoids (citral, carvone, menthone, camphor) as well as cyclohexanone and hex-5-en-2-one were subjected to transfer hydrogenation with PriOH/Raney nickel system at 82 or 150 °C. Among monoterpenoids, citral and carvone underwent full conversion at 82 °C within 5 h.

Radical chain reduction of alkylboron compounds with catechols

Villa, Giorgio,Povie, Guillaume,Renaud, Philippe

supporting information; experimental part, p. 5913 - 5920 (2011/06/16)

The conversion of alkylboranes to the corresponding alkanes is classically per-formed via protonolysis of alkylboranes. This simple reaction requires the use of severe reaction conditions, that is, treatment with a carboxylic acid at high temperature (>150 °C). We report here a mild radical procedure for the transformation of organoboranes to alkanes. 4-tert-Butylcatechol, a well-established radical inhibitor and antioxidant, is acting as a source of hydrogen atoms. An efficient chain reaction is observed due to the exceptional reactivity of phenoxyl radicals toward alkylboranes. The reaction has been applied to a wide range of organoboron derivatives such as B- alkylcatecholboranes, trialkylboranes, pinacolboronates, and alkylboronic acids. Furthermore, the so far elusive rate constants for the hydrogen transfer between secondary alkyl radical and catechol derivatives have been experimentally determined. Interestingly, they are less than 1 order of magnitude slower than that of tin hydride at 80 °C, making catechols particularly attractive for a wide range of transformations involving C-C bond formation.

Antimicrobial therapeutic compositions for oral and topical use

-

Page 7; 18, (2008/06/13)

The invention provides therapeutic antimicrobial compositions comprising natural phenolic compounds and essential oil alcohols and methods of use. The therapeutic antimicrobial compositions are useful to treat internal and external bacterial, fungal, and protozoan infections, as well as antibiotic resistant and secondary opportunistic infections.

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