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4-(bromomethyl)heptane, an alkyl halide with the molecular formula C8H17Br and a molecular weight of 197.12 g/mol, is a colorless liquid with a faint odor. It features a heptane backbone with a bromomethyl group attached to the fourth carbon atom. 4-(bromomethyl)heptane is insoluble in water but soluble in organic solvents, and is commonly used as a chemical intermediate in various industries.

101654-29-9

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101654-29-9 Usage

Uses

Used in Pharmaceutical Industry:
4-(bromomethyl)heptane is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules, contributing to the development of novel treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(bromomethyl)heptane serves as a chemical intermediate, aiding in the production of pesticides, herbicides, and other agricultural chemicals. Its reactivity and functional group make it a valuable component in the synthesis of these compounds.
Used in Organic Synthesis Research:
4-(bromomethyl)heptane is utilized as a reagent and reactant in organic synthesis research. Its versatility in forming new chemical bonds and participating in various reactions makes it an essential tool for scientists exploring new chemical pathways and developing innovative organic compounds.
Used in Industrial Applications:
4-(bromomethyl)heptane is also employed in industrial applications as a reactant in the production of various organic compounds. Its ability to undergo a range of chemical reactions makes it a valuable asset in the synthesis of specialty chemicals and materials.
Safety Precautions:
It is important to handle 4-(bromomethyl)heptane with care, as it is considered harmful if swallowed, inhaled, or in contact with skin. Additionally, it can cause irritation to the respiratory system and skin. Proper safety measures, such as wearing protective gear and working in well-ventilated areas, should be taken to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 101654-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,6,5 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 101654-29:
(8*1)+(7*0)+(6*1)+(5*6)+(4*5)+(3*4)+(2*2)+(1*9)=89
89 % 10 = 9
So 101654-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H17Br/c1-3-5-8(7-9)6-4-2/h8H,3-7H2,1-2H3

101654-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(bromomethyl)heptane

1.2 Other means of identification

Product number -
Other names 2-propyl-penta-1,4-diene

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:101654-29-9 SDS

101654-29-9Upstream product

101654-29-9Relevant articles and documents

Synthesis of GABA-valproic acid derivatives and evaluation of their anticonvulsant and antioxidant activity

Rekatas, George V.,Tani, Ekaterini,Demopoulos, Vassilis J.,Kourounakis, Panos N.

, p. 393 - 398 (1996)

The synthesis and the anticonvulsant activity of a number of GABA and valproic acid derivatives are reported. The lipophilicity of these compunds and their inhibitory effect on lipid peroxidation were also investigated, in an effort to correlate the anticonvulsant activity with lipophilicity and inhibitory effect on lipid peroxidation. The synthetized compounds exhibited anticonvulsant effects which were stronger for the more lipophilic derivatives. One of the active anticonvulsants showed appreciable antioxidant properties. Finally, a good correlation was found between the experimentally derived (R(M)) and calculated (Σf and log P(SK)) lipophilicity for this series of compounds.

Preparation of substituted cyclopentane and cyclopentene compounds and certain intermediates

-

Page column 11-12, (2008/06/13)

The invention relates to methods for preparing substituted cyclopentene compounds, their intermediates and use as neuraminidase inhibitors.

Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents

-

Page column 79, (2010/02/05)

This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.

Pheromones, 89.- Wittig Syntheses of Alkyl-Branched and Cyclic Analogs of (Z)-5-Decenyl Acetate, the Sex Pheromone of Agrotis segetum (Lepitoptera: Noctuidae)

Albores, Martha,Bestmann, Hans Juergen,Doehla, Bodo,Hirsch, Hans-Ludwig,Roesel, Peter,Vostrowsky, Otto

, p. 231 - 236 (2007/10/02)

By means of (Z)-selective Wittig olefination alkyl-branched and cyclic analogs of (Z)-5-decenyl acetate, the sex pheromone of the turnip moth, Agrotis segetum (Lepidoptera: Noctuidae), have been synthesized. Key Words: Pheromones / (Z)-5-decenyl acetate / Wittig reactions / Agrotis segetum

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