CAS 534-00-9

(2S)-1-Bromo-2-methylbutane

Description:

(2S)-1-Bromo-2-methylbutane is an organic compound classified as a haloalkane, specifically a bromoalkane, due to the presence of a bromine atom in its structure. It has a chiral center at the second carbon, which contributes to its stereochemistry, denoted by the (2S) configuration. This compound is characterized by its molecular formula, which includes carbon, hydrogen, and bromine atoms. It is typically a colorless liquid at room temperature and possesses a distinctive odor. The presence of the bromine atom makes it a polar molecule, influencing its solubility in various solvents; it is generally more soluble in organic solvents than in water. (2S)-1-Bromo-2-methylbutane can participate in nucleophilic substitution reactions, making it useful in organic synthesis. Its reactivity is influenced by the bromine atom, which can be replaced by nucleophiles in various chemical reactions. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.

Formula: C₅H₁₁Br

InChI: InChI=1S/C5H11Br/c1-3-5(2)4-6/h5H,3-4H2,1-2H3/t5-/m0/s1

InChI key: InChIKey=XKVLZBNEPALHIO-YFKPBYRVSA-N

SMILES: [C@@H](CBr)(CC)C

Synonyms:

• (+)-1-Bromo-2-methylbutane
• (+)-2-Methyl-1-bromobutane
• (+)-2-Methylbutyl bromide
• (2S)-1-Bromo-2-methylbutane
• (S)-(+)-2-Methyl-1-bromobutane
• (S)-(+)-2-Methylbutyl bromide
• 1-Bromo-2-(S)-methylbutane
• Butane, 1-bromo-2-methyl-, (2S)-
• Butane, 1-bromo-2-methyl-, (S)-
• d-Amyl bromide

(S)-(+)-1-Bromo-2-methylbutane, 97%, stab. with potassium carbonate

CAS: 534-00-9

(S)-(+)-1-Bromo-2-methylbutane, is used for the synthesis of chiral nematic liquid crystals and optically active Grignard reagents. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legac

Formula: C₅H₁₁Br

Purity: 97%

Color and Shape: Clear colorless to yellow, Liquid

Molecular weight: 151.05

Ref: 02-H27078

(S)-(+)-1-Bromo-2-methylbutane

CAS: 534-00-9

(S)-(+)-1-Bromo-2-methylbutane

Formula: C₅H₁₁Br

Purity: 97%

Molecular weight: 151.04

Ref: 54-OR1043074

(S)-(+)-1-Bromo-2-Methylbutane

CAS: 534-00-9

Purity: 97%

Ref: IN-DA01DQA9

(S)-1-Bromo-2-methylbutane

CAS: 534-00-9

(S)-1-Bromo-2-methylbutane

Formula: C₅H₁₁Br

Purity: 97% (stabilized with potassium carbonate)

Molecular weight: 151.04

Ref: IN-DG48203

(S)-1-Bromo-2-methylbutane

CAS: 534-00-9

Purity: 98%

Color and Shape: Liquid (Oil)

Molecular weight: 150.004

Ref: 10-F569508

(S)-(+)-1-Bromo-2-methylbutane

CAS: 534-00-9

(S)-(+)-1-Bromo-2-methylbutane is a chiral molecule with two stereoisomers, the cis and trans forms. The cis form has been observed to be the more stable of the two. It is a functional theory that these two forms are not mirror images of each other because they have different conformations. (S)-(+)-1-Bromo-2-methylbutane has been used in the synthesis of a number of important molecules. The stereoisomers can be distinguished by conformational analysis and optical microscopy. (S)-(+)-1-Bromo-2-methylbutane also has an application in biotechnology for use as a precursor for hydrazones, which are important in organic chemistry and molecular biology, such as DNA sequencing.

Formula: C₅H₁₁Br

Purity: Min. 95%

Molecular weight: 151.04 g/mol

Ref: 3D-AAA53400