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1,3-Dibromo-2-nonanone is an organic compound with the chemical formula C9H16Br2O. It is a colorless liquid with a molecular weight of 312.03 g/mol. 1,3-Dibromo-2-nonanone is characterized by the presence of two bromine atoms attached to the first and third carbon atoms of a nonanone (a nine-carbon ketone) backbone. The bromine atoms are in a vicinal (adjacent) position, which can influence its chemical reactivity and properties. 1,3-Dibromo-2-nonanone is used in various chemical synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. It is important to handle 1,3-Dibromo-2-nonanone with care due to its potential toxicity and reactivity.

1982-80-5

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1982-80-5 Usage

Type of compound

Synthetic organic compound

Primary uses

Flavoring agent and fragrance ingredient

Odor

Strong, sweet

Applications

Production of food flavorings and perfumes

Additional property

Antimicrobial

Popular in

Personal care products (soaps and cosmetics)

Safety concerns

Classified as a skin and eye irritant

Potential issues

May cause allergic reactions in some individuals

Precaution

Use with caution due to irritant and allergenic properties

Check Digit Verification of cas no

The CAS Registry Mumber 1982-80-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1982-80:
(6*1)+(5*9)+(4*8)+(3*2)+(2*8)+(1*0)=105
105 % 10 = 5
So 1982-80-5 is a valid CAS Registry Number.

1982-80-5Downstream Products

1982-80-5Relevant academic research and scientific papers

Halogen chemistry of the red alga Bonnemaisonia

McConnell, Oliver J.,Fenical, William

, p. 233 - 247 (2007/10/10)

Complete accounts of the natural products chemistry of Bonnemaisonia nootkana, B. asparagoides, B. hamifera and Trailliella intricata are described. In contrast to the chemistry of the closely related alga Asparagopsis, Bonnemaisonia spp. do not produce halomethanes, but instead an array of C7-C9 halogen-containing ketones, alcohols and carboxylic acids. Biomimetic syntheses of these compounds suggest they are precursors and products of in vivo Favorsky rearrangements.

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