53353-01-8 Usage
Description
(S)-(+)-1-BROMO-4-METHYLHEXANE, with the molecular formula C7H15Br, is a chiral chemical compound that exists in two non-superimposable mirror image forms known as enantiomers. (S)-(+)-1-BROMO-4-METHYLHEXANE is characterized by its strong alkylating properties, which arise from the presence of the bromine atom. It is widely utilized in organic synthesis and serves as a fundamental building block for the creation of various pharmaceuticals and agrochemicals. Furthermore, (S)-(+)-1-BROMO-4-METHYLHEXANE is employed in the development of innovative materials and for research purposes. However, it is crucial to handle this compound with care due to its toxic nature and potential health risks if mismanaged.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-1-BROMO-4-METHYLHEXANE is used as a key intermediate in the synthesis of various pharmaceuticals for [application reason], such as the development of new drugs and the improvement of existing medications. Its unique chemical properties make it a valuable asset in the design and production of a wide range of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-(+)-1-BROMO-4-METHYLHEXANE is used as a building block for the production of different agrochemicals for [application reason], including the creation of novel pesticides and herbicides. Its alkylating properties contribute to the effectiveness of these products in controlling pests and weeds.
Used in Material Science:
(S)-(+)-1-BROMO-4-METHYLHEXANE is utilized as a component in the development of new materials for [application reason], such as advanced polymers and composites. Its unique chemical structure allows for the creation of materials with enhanced properties, such as improved strength, durability, and resistance to various environmental factors.
Used in Research and Development:
(S)-(+)-1-BROMO-4-METHYLHEXANE is also employed in research and development for [application reason], where it aids in the exploration of new chemical reactions and processes. Its strong alkylating properties make it an essential tool for understanding and advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 53353-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53353-01:
(7*5)+(6*3)+(5*3)+(4*5)+(3*3)+(2*0)+(1*1)=98
98 % 10 = 8
So 53353-01-8 is a valid CAS Registry Number.
53353-01-8Relevant articles and documents
New syntheses of 1,7-dimethylnonyl propanoate, the western corn rootworm pheromone, in four different ways via cross metathesis, alkylation and coupling reactionsss
Mori, Kenji
experimental part, p. 595 - 600 (2011/04/23)
A mixture of the four stereoisomers of 1,7-dimethylnonyl propanoate, the female sex pheromone of the western corn rootworm (Diabrotica virgifera virgifera LeConte), was synthesized in four different ways by employing one of the following four reactions as the key step: (i) cross metathesis using the Grubbs I catalyst, (ii) cross metathesis using the Grubbs II catalyst, (iii) alkylation of an alkynide anion, and (iv) Grignard coupling in the presence of dilithium tetrachlorocuprate. Although the cross metathesis approaches enabled two short syntheses (4 or 6 steps) of the pheromone to be achieved, the cheapest and most efficient synthesis was possible via Grignard coupling to give the desired pheromone in a 40% overall yield based on 2-methyl-1-butanol (8 steps).
48. Ferroelectric Liquid Crystals Part 2 Chiral Phenyl Benzoates Incorporating a trans-1,4-Disubstituted Cyclohexane Ring
Kelly, Stephen M.,Buchecker, Richard
, p. 451 - 460 (2007/10/02)
About forty novel phenyl benzoates also incorporating a trans-1,4-disubstituted cyclohexane ring and a chiral centre have been prepared.The dependence of the liquid-crystal transition temperatures of this new class of compounds on lateral substituents, diverse central linkages, chain lengths, and position of the chiral centre has been studied systematically.The synthesis and liquid-crystal transition temperatures of these new compounds are described in detail.
SYNTHESIS AND BIOLOGICAL ACTIVITY OF BOTH (E)- AND (Z)-ISOMERS OF OPTICALLY PURE (S)-14-METHYL-8-HEXADECENAL (TROGODERMAL), THE ANTIPODES OF THE PHEROMONE OF THE KHAPRA BEETLE
Mori, K.,Kuwahara, S.,Levinson, H. Z.,Levinson, A. R.
, p. 2291 - 2297 (2007/10/02)
Both (E)- and (Z)-isomers of (S)-14-methyl-8-hexadecenal (trogodermal) were synthesized from 100percent optically pure (R)-(+)-citronellic acid.These antipodes of the khapra beetle pheromone were 1/500 to 1/1000 times as active as the natural (R)-pheromone.Determination of the optical purities of citronellic acid and related compounds was achieved by hplc method.Warning was made not to forget the measurement of density in expressing the optical rotation of a neat liquid as D (neat).
