Molecular Biology Reagents

1-Bromo-3-chloropropane is a solvent that has been described as a less toxic replacement for chloroform in the liquid-phase separation and isolation of RNA from DNA and proteins. 1-Bromo-3-chloropropane is described to be efficacious in the

1-Bromo-4-chloro-3-(morpholinocarbonyl)benzene.

1-Bromo-4-chloro-3-(morpholinocarbonyl)benzene.

Usually used in the synthesis of 4-tert-butyl-phenylboronic acid, 1-deoxy analogs of CP-47,497 (n = 0 to 7) and 1-deoxy analogs of CP-55,940 (n = 0 to 7).

Usually used in the synthesis of 4-tert-butyl-phenylboronic acid, 1-deoxy analogs of CP-47,497 (n = 0 to 7) and 1-deoxy analogs of CP-55,940 (n = 0 to 7).

Usually used in the synthesis of 4-tert-butyl-phenylboronic acid, 1-deoxy analogs of CP-47,497 (n = 0 to 7) and 1-deoxy analogs of CP-55,940 (n = 0 to 7).

Usually used in the synthesis of 4-tert-butyl-phenylboronic acid, 1-deoxy analogs of CP-47,497 (n = 0 to 7) and 1-deoxy analogs of CP-55,940 (n = 0 to 7).

1-Bromo-5-methylhexane.

1-Bromo-5-methylhexane.

1-Bromo-5-methylhexane.

1-Bromo-5-methylhexane.

1-Bromopinacolone is an α-bromoketone-aldehyde. Coupling of 1-bromopinacolone with various aldehyde electrophiles catalyzed by SmI2 has been reported. It acts as reversible competitive inhibitor for acetylcholinesterase, during hydrolysis of