1256360-46-9

1256360-46-9 - Names and Identifiers

Name	1-[(4-Methylphenyl)sulfonyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine
Synonyms	1-Tosyl-1,2,3,6-tetrahydropyridine-4-boronic acid, pinacol ester (1-TOSYL-1,2,3,6-TETRAHYDROPYRIDIN-4-YL)BORONIC ACID PINACOL ESTER 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1,2,3,6-tetrahydropyridine 1-(4-methylphenyl)sulfonyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine 1-(4-methylbenzenesulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine 1-[(4-Methylphenyl)sulfonyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine Pyridine, 1,2,3,6-tetrahydro-1-[(4-methylphenyl)sulfonyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS	1256360-46-9
InChI	InChI=1S/C18H26BNO4S/c1-14-6-8-16(9-7-14)25(21,22)20-12-10-15(11-13-20)19-23-17(2,3)18(4,5)24-19/h6-10H,11-13H2,1-5H3

1256360-46-9 - Physico-chemical Properties

Molecular Formula	C18H26BNO4S
Molar Mass	363.28
Density	1.2±0.1 g/cm3
Boling Point	444.2±55.0 °C at 760 mmHg
Flash Point	222.5±31.5 °C
Vapor Presure	0.0±1.1 mmHg at 25°C
Storage Condition	Sealed in dry,Store in freezer, under -20°C
Sensitive	IRRITANT
Refractive Index	1.558
MDL	MFCD17926518

1256360-46-9 - Introduction

4-(4,4, 5,5-tetramethyl-[1,3,2] dioxaborolan-2-yl)-1-(toluene-4-sulfonyl)-1,2,3,6-tetrahydropyridine is an organic compound with a variety of properties and uses.

Nature:
-Appearance: A white to off-white crystalline solid.
-Melting point: about 125-130°C.
-Solubility: Soluble in common organic solvents (such as methanol, ethanol, chloroform, etc.), but insoluble in water.
-Stability: relatively stable under conventional conditions, but can be decomposed or discolored by heat.
-Chemical properties: As a derivative of pyridine, it has similar chemical reactivity to pyridine.

Use:
-Catalyst: This compound can be used as a precursor of a coordination compound catalyst to participate in various organic synthesis reactions, such as hydrogenation reactions, arylene alkene reactions, etc.
-Research field: Due to its special structure and reaction properties, the compound is widely used in the fields of organic synthesis, coordination chemistry and materials science.

Method:
The synthesis method of the compound is relatively complex, generally using multi-step reaction, including ring reaction, substitution reaction, coordination reaction and so on.

Safety Information:
-The compound is not specifically classified as a hazardous substance, but it is still necessary to pay attention to safe handling measures, such as wearing protective gloves, safety glasses, etc.
-Avoid contact and inhalation of the compound and avoid swallowing.
-Avoid contact of the compound with skin, eyes and mucous membranes. If contact occurs, rinse immediately with plenty of water and seek medical help.
-storage should be sealed, stored in a dark, dry place.

Last Update：2024-04-09 21:04:16