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1,4-Dibromobutane-1,1,4,4-D4 (CAS# 36684-45-4) is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of 1,4-dibromobutane with deuterium atoms replacing four hydrogen atoms, which can provide valuable insights into the behavior and properties of the molecule in different chemical and biological contexts.

36684-45-4

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36684-45-4 Usage

Uses

Used in Chemical Research:
1,4-Dibromobutane-1,1,4,4-D4 is used as a research compound for studying the effects of isotopic labeling on the chemical properties and reactivity of 1,4-dibromobutane. The presence of deuterium atoms can help researchers understand the influence of isotopic substitution on reaction rates, mechanisms, and product distributions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1,4-Dibromobutane-1,1,4,4-D4 is used as a labeled compound for investigating the metabolism and pharmacokinetics of related drug molecules. The deuterium labeling can provide information on the metabolic pathways and help in the development of more effective and safer drugs.
Used in Environmental Studies:
1,4-Dibromobutane-1,1,4,4-D4 can be employed as a tracer compound in environmental research to study the fate and transport of 1,4-dibromobutane and its analogs in the environment. The isotopic labeling can help in tracking the compound's behavior in various environmental matrices, such as water, soil, and air, and provide insights into its persistence, degradation, and potential impact on ecosystems.
Used in Material Science:
In material science, 1,4-Dibromobutane-1,1,4,4-D4 can be utilized as a component in the synthesis of novel materials with specific properties. The isotopic labeling can help in understanding the structure-property relationships and guide the design of new materials with tailored characteristics for various applications.
Overall, 1,4-Dibromobutane-1,1,4,4-D4 is a versatile isotopically labeled compound with applications in various fields, including chemical research, pharmaceutical research, environmental studies, and material science. Its use in these areas can contribute to a better understanding of the underlying processes and lead to the development of innovative solutions and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 36684-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,6,8 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36684-45:
(7*3)+(6*6)+(5*6)+(4*8)+(3*4)+(2*4)+(1*5)=144
144 % 10 = 4
So 36684-45-4 is a valid CAS Registry Number.

36684-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-DIBROMOBUTANE-1,1,4,4-D4

1.2 Other means of identification

Product number -
Other names 1,4-dibromobicyclo<2.2.1>heptane

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:36684-45-4 SDS

36684-45-4Relevant academic research and scientific papers

Formation of RuII-alkyl-butadiene complexes from dihalogeno-RuIV-allyl precursors by the reaction with BrMg(CH2)4MgBr: a novel decomposition pathway for ruthena(IV)cyclopentane intermediates

Nagashima, Hideo,Michino, Yoshiyuki,Ara, Ken-ichi,Fukahori, Takahiko,Itoh, Kenji

, p. 189 - 196 (2007/10/02)

Treatment of (C5Me5)RuBr2(η3-CH2C(R)CH2) with BrMg(CH2)4MgBr in ether afforded the RuII-alkyl-butadiene complexes, (C5Me5)Ru(η4-C4H6)(η1-Ch2CHRCH3) .Labeling experiments have revealed a mechanism involving a double β-hydrogen elimination from ruthenacyclopentane intermediates and subsequent stepwise transfer of the hydrogen atoms to hydrogenate the η3-allyl ligand.

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