2-Bromo-4-methyl-benzothiol, with the CAS number 14395-53-0, is an organic compound that features a benzothiol structure, which consists of a benzene ring fused to a thiol (sulfhydryl) group. The presence of a bromine atom at the second position and a methyl group at the fourth position of the benzene ring contributes to its unique chemical properties. This compound is typically characterized by its aromatic nature, which imparts stability and distinct reactivity patterns, particularly in electrophilic substitution reactions. The thiol group (-SH) is known for its nucleophilic characteristics, making the compound reactive towards electrophiles. Additionally, the bromine substituent can facilitate further chemical transformations, such as nucleophilic substitution or coupling reactions. 2-Bromo-4-methyl-benzothiol may be utilized in various applications, including organic synthesis, pharmaceuticals, and as a potential intermediate in the production of other chemical compounds. Safety considerations should be taken into account due to the presence of bromine and the thiol group, which can be toxic and malodorous.

2-BROMO-4-METHYL-BENZOTHIOL

14395-53-0: 2-Bromo-4-methylbenzyl thiol, 2-Bromo-4-Methylbenzenethiol

(1S)-2,2,2-Trifluoro-1-phenylethanamine is a six-membered heterocycle with enhancements in six of the eight possible dihedral angles. The molecule has four hydrogen bonds (two intramolecular, two intermolecular). There is one dipole moment and one bonding frequency. The molecule has strong intramolecular hydrogen bonding due to its chelate ring formation and four of the five possible intramolecular hydrogen bonds.

CAS 14395-53-0: 2-BROMO-4-METHYL-BENZOTHIOL

(1S)-2,2,2-Trifluoro-1-Phenylethanamine

Ref: 3D-FT84820

2-Bromo-4-methylbenzenethiol

Ref: 10-F037914

2-Bromo-4-methyl-benzenethiol

Ref: 54-OR97372