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2,3-Dibromohexanal, also known as 2,3-dibromo-6-aldehyde, is an organic compound characterized by the molecular formula C6H10Br2O. It presents as a colorless to pale yellow liquid with a distinctive strong, pungent odor. This chemical is recognized for its role as an intermediate in the synthesis of pharmaceuticals and other organic compounds, as well as its utility as a chemical reagent in laboratory experiments. Additionally, 2,3-dibromohexanal has demonstrated antimicrobial properties, which are currently under investigation for potential applications as a preservative in food and cosmetic products. Due to its potential hazards upon inhalation, ingestion, or skin contact, careful handling of this chemical is advised.

99414-71-8

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99414-71-8 Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-Dibromohexanal is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Organic Compound Synthesis:
This chemical serves as an intermediate in the synthesis of other organic compounds, playing a crucial role in the creation of a wide range of chemical products.
Used in Laboratory Experiments:
2,3-Dibromohexanal is employed as a chemical reagent in various laboratory settings, facilitating research and experimentation across different scientific disciplines.
Used in Agricultural and Industrial Settings:
With its demonstrated antimicrobial properties, 2,3-dibromohexanal has potential applications in agriculture and industry, where it could be used for its preservative qualities.
Used as a Preservative in Food and Cosmetic Products:
2,3-Dibromohexanal is being studied for its potential use as a preservative in food and cosmetic products, capitalizing on its antimicrobial properties to extend shelf life and maintain product integrity.

Check Digit Verification of cas no

The CAS Registry Mumber 99414-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,1 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99414-71:
(7*9)+(6*9)+(5*4)+(4*1)+(3*4)+(2*7)+(1*1)=168
168 % 10 = 8
So 99414-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10Br2O/c1-2-3-5(7)6(8)4-9/h4-6H,2-3H2,1H3

99414-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dibromohexanal

1.2 Other means of identification

Product number -
Other names Hexanal,2,3-dibromo

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:99414-71-8 SDS

99414-71-8Upstream product

99414-71-8Downstream Products

99414-71-8Relevant academic research and scientific papers

Enantioselective Preparation of Polyfunctional Secondary Allylic Alcohols Using Functionalized Dialkylzincs Prepared by a Copper(I) Catalyzed Iodine-Zinc Exchange Reaction.

Rozema, Michael J.,Eisenberg, Christina,Luetjens, Henning,Ostwald, Roswitha,Belyk, Kevin,Knochel, Paul

, p. 3115 - 3118 (1993)

Catalytic amounts of Cu(I) salts considerably facilitate the iodine-zinc exchange reaction leading to polyfunctional dialkylzincs.The catalytic asymmetric addition of these zinc reagents to a wide range of α,β-unsaturated aldehydes provides polyfunctional allylic alcohols with a high enantioselectivity.

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