41242-50-6 Usage
General Description
2-Bromo-2-methylbutyric acid is a compound with the molecular formula C5H9BrO2. It is a colorless liquid with a molecular weight of 175.03 g/mol. This chemical is used as a building block in the synthesis of pharmaceuticals and agrochemicals, and is also used as a reagent in organic synthesis. It is known for its strong and unpleasant odor, and is classified as a hazardous substance. Additionally, 2-Bromo-2-methylbutyric acid has the potential to cause skin and eye irritation, and is harmful if ingested or inhaled. Therefore, proper handling and storage of this compound is essential to prevent any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 41242-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,4 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41242-50:
(7*4)+(6*1)+(5*2)+(4*4)+(3*2)+(2*5)+(1*0)=76
76 % 10 = 6
So 41242-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9BrO2/c1-3-5(2,6)4(7)8/h3H2,1-2H3,(H,7,8)
41242-50-6Relevant articles and documents
CERAMIDE GALACTOSYLTRANSFERASE INHIBITORS FOR THE TREATMENT OF DISEASE
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Paragraph 000820; 000821, (2018/01/17)
Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme ceramide galactosyltransferase (CGT), such as, for example, lysosomal storage diseases. Examples of lysosomal storage diseases include, for example, Krabbe disease and Metachromatic Leukodystrophy.
Indium-mediated Reformatsky-Claisen rearrangement
Ishihara, Jun,Watanabe, Yuki,Koyama, Noriko,Nishino, Yukihiro,Takahashi, Keisuke,Hatakeyama, Susumi
body text, p. 3659 - 3667 (2011/06/21)
A new variant of the Reformatsky-Claisen rearrangement is described. The reaction of substituted allyl α-bromoacetates with indium and indium(III) chloride under ultrasonication provides a general entry into the functionalized synthon.
