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1-BROMO-5-METHYLHEPTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54089-01-9

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54089-01-9 Usage

Classification

Alkyl bromide

Structure

Seven-carbon chain with a methyl group and a bromine atom attached to one of the carbon atoms

Uses

Intermediate in organic synthesis, production of pharmaceuticals and agrochemicals

Application

Solvent in chemical reactions, reagent in organic chemistry

Function

Alkylating agent in various chemical processes and research applications

Hazards

Flammability and toxicity, requires cautious handling

Check Digit Verification of cas no

The CAS Registry Mumber 54089-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54089-01:
(7*5)+(6*4)+(5*0)+(4*8)+(3*9)+(2*0)+(1*1)=119
119 % 10 = 9
So 54089-01-9 is a valid CAS Registry Number.

54089-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-5-methylheptane

1.2 Other means of identification

Product number -
Other names 5-methyl-1-bromoheptane

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:54089-01-9 SDS

54089-01-9Upstream product

54089-01-9Relevant academic research and scientific papers

Novel fatty acid methyl esters from the actinomycete Micromonospora aurantiaca

Dickschat, Jeroen S.,Bruns, Hilke,Riclea, Ramona

, p. 1697 - 1712 (2012/02/04)

The volatiles released by Micromonospora aurantiaca were collected by means of a closed-loop stripping apparatus (CLSA) and analysed by GC-MS. The headspace extracts contained more than 90 compounds from different classes. Fatty acid methyl esters (FAMEs) comprised the major compound class including saturated unbranched, monomethyl and dimethyl branched FAMEs in diverse structural variants: Unbranched, α-branched, γ-branched, (ω-1)-branched, (ω-2)-branched, α-and (ω-1)-branched, γ-and (ω-1)-branched, γ-and (ω-2)-branched, and γ-and (ω-3)-branched FAMEs. FAMEs of the last three types have not been described from natural sources before. The structures for all FAMEs have been suggested based on their mass spectra and on a retention index increment system and verified by the synthesis of key reference compounds. In addition, the structures of two FAMEs, methyl 4,8-dimethyldodecanoate and the ethyl-branched compound methyl 8-ethyl-4-methyldodecanoate were deduced from their mass spectra. Feeding experiments with isotopically labelled [ 2H10]leucine, [2H10]isoleucine, [2H8]valine, [2H5]sodium propionate, and [methyl-2H3]methionine demonstrated that the responsible fatty acid synthase (FAS) can use different branched and unbranched starter units and is able to incorporate methylmalonyl-CoA elongation units for internal methyl branches in various chain positions, while the methyl ester function is derived from S-adenosyl methionine (SAM).

SYNTHETIC INVESTIGATIONS INTO INSECT-ATTRACTING SUBSTANCES (SEX ATTRACTANTS). IV. SYNTHESIS OF 14-METHYL-8-cis-HEXADECENAL AND 14-METHYL-8-trans-HEXADECENAL, COMPONENTS OF THE SEX PHEROMONE OF THE DERMESTID BEETLE Trogoderma granarium EVERTS

Kovalev, B. G.,Rastegaeva, V. M.

, p. 44 - 47 (2007/10/02)

14-Methyl-8-hexadecyn-1-ol was obtained by the alkylation of 7-methyl-1-nonyne with heptamethylene chlorohydrin.Its hydrogenation in the presence of colloidal nickel catalyst was used for the synthesis of 14-methyl-8-cis-hexadecen-1-ol, and reduction with lithium aluminum hydride was used for the synthesis of 14-methyl-8-trans-hexadecen-1-ol.Both ethylenic alcohols were converted by oxidation into the corresponding aldehydes, which are the main components of the sex pheromone of the dermestid beetle.

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