7357-56-4 Usage
Uses
Used in Organic Synthesis:
Methyl 2-Bromodecanoate is used as a chemical intermediate for the synthesis of various organic compounds. Its bromo functional group allows it to participate in a wide range of chemical reactions, making it a valuable component in the production of different chemicals.
Used in Pharmaceutical Production:
Methyl 2-Bromodecanoate is used as a starting material or intermediate in the synthesis of pharmaceuticals. Its versatility in chemical reactions enables the creation of new drug molecules with potential therapeutic applications.
Used in Perfume Industry:
Methyl 2-Bromodecanoate is used as a component in the production of perfumes. Its unique chemical properties contribute to the creation of various fragrances and scents, enhancing the overall sensory experience of the final product.
Safety Precautions:
Handling Methyl 2-Bromodecanoate requires caution as it can cause skin and eye irritation upon contact. It may also have harmful effects if inhaled or swallowed. Therefore, appropriate safety measures should be taken during its storage, handling, and disposal to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 7357-56-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7357-56:
(6*7)+(5*3)+(4*5)+(3*7)+(2*5)+(1*6)=114
114 % 10 = 4
So 7357-56-4 is a valid CAS Registry Number.
7357-56-4Relevant academic research and scientific papers
One-pot oxidative bromination – Esterification of aldehydes to 2-bromoesters using cerium (IV) ammonium nitrate and lithium bromide
Nikishin, Gennady I.,Kapustina, Nadezhda I.,Sokova, Lyubov L.,Bityukov, Oleg V.,Terent'ev, Alexander O.
supporting information, p. 352 - 354 (2017/01/03)
A two-step, one-pot reaction of aldehydes with the CAN/LiBr oxidation system under solvent-free conditions followed by the addition of methanol affords methyl α-bromocarboxylates. The oxidation of aldehydes with methanol using this system gives only methyl esters. A facile method, which does not require special equipment, was developed for the synthesis of 2-bromoesters from aliphatic aldehydes with carbon chain lengths of 5–10 atoms.
SOLVOLYSIS OF 1-CHLORO-1-ALKENYL PHENYL SULFIDES. SYNTHESIS OF α-BROMO PHENYL THIOCARBOXYLIC ESTERS, α-BROMO ALKYL CARBOXYLIC ESTERS AND α-PHENYLTHIO METHYL CARBOXYLIC ESTERS
Fortes, C. C.,Chaves, M. H.
, p. 751 - 762 (2007/10/02)
1-Chloro-1-alkenyl phenyl sulfides treated with bromine followed by hydrolysis or methanolysis give α-bromo phenyl thiocarboxylic esters and α-phenylthio methyl carboxylic esters.Direct oxidative solvolysis with bromine and alcohol give α-bromo alkyl carboxylic esters.
