CAS 1415841-82-5

Formula: C10H16BrNO2

InChI: InChI=1S/C10H16BrNO2/c1-10(2,3)14-9(13)12-6-4-5-8(11)7-12/h5H,4,6-7H2,1-3H3

InChI key: OCGCRVVGDPPGMC-UHFFFAOYSA-N

SMILES: CC(C)(C)OC(=O)N1CCC=C(C1)Br

tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

CAS: 1415841-82-5

tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

Formula: C₁₀H₁₆BrNO₂

Purity: 97%

Molecular weight: 262.14

Ref: 54-OR79582

tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

CAS: 1415841-82-5

Formula: C₁₀H₁₆BrNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 262.1435

Ref: IN-DA001GMK

tert-Butyl 3-bromo-5,6-dihydropyridine-1(2H)-carboxylate

CAS: 1415841-82-5

tert-Butyl 3-bromo-5,6-dihydropyridine-1(2H)-carboxylate

Formula: C₁₀H₁₆BrNO₂

Purity: 98%

Molecular weight: 262.14

Ref: IN-DG758431

tert-Butyl 5-bromo-1,2,3,6-tetrahydropyridine-1-carboxylate

CAS: 1415841-82-5

Formula: C₁₀H₁₆BrNO₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 262.147

Ref: 10-F517311

1-N-Boc-5-bromo-3,6-dihydro-2H-pyridine

CAS: 1415841-82-5

1-N-Boc-5-bromo-3,6-dihydro-2H-pyridine is an alkaloid that is used as a precursor for the synthesis of other compounds. This compound can be obtained from the reaction of ethylmagnesium bromide and 1,2,4,5 tetraisopropoxy benzene. The 1,2,4,5 tetraisopropoxybenzene reacts with titanium tetrachloride to yield 1-N-Boc-5-bromo-3,6 dihydro 2H pyridine. 1-N-Boc 5 bromo 3,6 dihydro 2H pyridine can also be obtained by the reduction of 1 N Boc 5 bromo 3,6 dihydro 2H pyridinium chloride with sodium sulfonate in a high yield. The nitrogen atom in this compound is stere

Formula: C₁₀H₁₆BrNO₂

Purity: Min. 95%

Molecular weight: 262.15 g/mol

Ref: 3D-QGC84182