99414-72-9 Usage
Explanation
The chemical formula of 2,3-dibromo-3-methylbutanal consists of 5 carbon atoms, 8 hydrogen atoms, 2 bromine atoms, and 1 oxygen atom.
Explanation
2,3-dibromo-3-methylbutanal appears as a pale yellow liquid in its pure form.
Explanation
This chemical compound has a noticeable and pungent odor.
Explanation
2,3-dibromo-3-methylbutanal is used to provide a buttery and caramel-like aroma in food products.
Explanation
In perfumes and personal care products, this compound adds a warm and sweet scent.
Explanation
2,3-dibromo-3-methylbutanal easily vaporizes and releases fumes at room temperature.
Explanation
This chemical compound can easily catch fire and burn, posing a potential hazard.
Explanation
Due to its volatility and flammability, it is important to handle 2,3-dibromo-3-methylbutanal carefully and ensure proper ventilation to minimize health risks.
Explanation
Exposure to 2,3-dibromo-3-methylbutanal may pose health hazards, so it is crucial to follow safety guidelines when working with this chemical.
Physical state
Pale yellow liquid
Odor
Strong, pungent
Usage in food industry
Flavoring agent
Usage in fragrance industry
Warm, sweet note
Volatility
Volatile
Flammability
Flammable
Safety precautions
Handle with caution in well-ventilated areas
Health hazards
Potential health risks
Check Digit Verification of cas no
The CAS Registry Mumber 99414-72-9 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 99414-72:
(7*9)+(6*9)+(5*4)+(4*1)+(3*4)+(2*7)+(1*2)=169
169 % 10 = 9
So 99414-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H8Br2O/c1-5(2,7)4(6)3-8/h3-4H,1-2H3
99414-72-9Relevant articles and documents
Preparation of α-haloacrylate derivatives via dimethyl sulfoxide-mediated selective dehydrohalogenation
Li, Wei,Li, Jianchang,Wan, Zhao-Kui,Wu, Junjun,Massefski, Walter
, p. 4607 - 4610 (2008/03/13)
(Chemical Equation Presented) Dimethyl sulfoxide causes α/β-dihalopropanoate derivatives to undergo efficient, selective dehydrohalogenation to form α-haloacrylate analogues. A variety of α-halo Michael acceptors were prepared in dimethyl sulfoxide under mild, base-free conditions, including the preparation of α-bromoacrolein and α-chloro- and bromoacrylonitriles. Synthesis of these molecules has been reported in the literature to be difficult. Among all the existing dehydrohalogenation procedures, this protocol is the most facile, practical, and environmentally benign process.
