CAS 51857-17-1

N-BOC-1,6-diaminohexane

Description:

N-BOC-1,6-diaminohexane, also known as tert-butoxycarbonyl-1,6-diaminohexane, is an organic compound characterized by the presence of two amino groups (-NH2) and a tert-butoxycarbonyl (BOC) protecting group. This compound features a hexane backbone, which contributes to its aliphatic nature. The BOC group is commonly used in organic synthesis to protect amines during chemical reactions, allowing for selective functionalization. N-BOC-1,6-diaminohexane is typically a white to off-white solid and is soluble in polar organic solvents. Its structure allows for potential applications in peptide synthesis and drug development, particularly in the formation of amide bonds. The presence of two amino groups makes it a versatile building block for creating more complex molecules. As with many amines, it may exhibit basic properties and can participate in various chemical reactions, including acylation and coupling reactions. Proper handling and storage are essential due to its reactivity and potential hazards associated with amines.

Formula: C₁₁H₂₄N₂O₂

InChI: InChI=1S/C11H24N2O2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8-12/h4-9,12H2,1-3H3,(H,13,14)

InChI key: InChIKey=RVZPDKXEHIRFPM-UHFFFAOYSA-N

SMILES: C(NCCCCCCN)(OC(C)(C)C)=O

Synonyms:

• (6-Aminohexyl)carbamic acid tert-butyl ester
• 1-((tert-Butoxycarbonyl)amino)-6-aminohexane
• 6-((tert-Butoxycarbonyl)amino)-1-hexylamine
• 6-(tert-Butoxycarbonyl)amino-1-aminohexane
• 6-(tert-Butoxycarbonylamino)-1-hexanamine
• 6-(tert-Butoxycarbonylamino)hexylamine
• 6-Aminohexylcarbamic acid tert-butyl ester
• 6-[(Tert-Butoxycarbonyl)Amino]Hexan-1-Aminium
• 6-[(tert-Butyloxycarbonyl)amino]hexylamine
• Boc-1,6-hexanediamine
• Carbamic acid, (6-aminohexyl)-, 1,1-dimethylethyl ester
• Carbamic acid, N-(6-aminohexyl)-, 1,1-dimethylethyl ester
• Mono-BOC-hexamethylenediamine
• N-(tert-Butoxycarbonyl)-1,6-diaminohexane
• N-(tert-Butoxycarbonyl)hexamethylenediamine
• N-Boc-1,6-Hexanediamine
• N-Boc-1,6-diaminohexane
• Tert-Butyl (6-Aminohexyl)Carbamate
• tert-Butyl N-(6-aminohexyl)carbamate
• tert-Butyloxycarbonyl-1,6-hexamethylenediamine

N-(tert-Butoxycarbonyl)-1,6-diaminohexane

CAS: 51857-17-1

Formula: C₁₁H₂₄N₂O₂

Purity: >98.0%(T)

Color and Shape: Colorless to Yellow to Orange clear liquid

Molecular weight: 216.33

Ref: 3B-A1375

N-Boc-1,6-diaminohexane, 98%

CAS: 51857-17-1

N-Boc-1,6-diaminohexane is used to prepare 1,3-Bis[6-(Boc-amino)hexyl]urea by reacting with carbonyl dichloride in the presence of triethylamine. Further, it is used as a reagent for the introduction of a C6-spacer. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar

Formula: C₁₁H₂₅N₂O₂

Purity: 98%

Color and Shape: Clear colorless to pale yellow, Liquid or viscous liquid

Molecular weight: 217.33

Ref: 02-L19948

N-tert-Butoxycarbonyl-1,6-hexanediamine

CAS: 51857-17-1

Formula: C₁₁H₂₄N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 216.3205

Ref: IN-DA0035EZ

NH2-C6-NH-Boc

CAS: 51857-17-1

NH2-C6-NH-Boc

Purity: ≥98%

Molecular weight: 216.32g/mol

Ref: 54-BUP19659

n-boc-1,6-Hexane diamine

CAS: 51857-17-1

n-boc-1,6-Hexane diamine

Formula: C₁₁H₂₄N₂O₂

Purity: 98%

Color and Shape: light yellow liquid

Molecular weight: 216.32g/mol

Ref: 54-OR345618

NH2-C6-NH-Boc

CAS: 51857-17-1

NH2-C6-NH-Boc is a PROTAC linker. NH2-C6-NH-Boc can be used in the synthesis the Mcl-1 inhibitor based on PROTAC.

Formula: C₁₁H₂₄N₂O₂

Purity: 99.97%

Color and Shape: Clear Light Yellow Viscous Liquid

Molecular weight: 216.32

Ref: TM-T18487

N-Boc-1,6-Diaminohexane

CAS: 51857-17-1

Formula: C₁₁H₂₄N₂O₂

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 216.325

Ref: 10-F077278

N-Boc-1,6-diaminohexane

Controlled Product

CAS: 51857-17-1

Applications N-Boc-1,6-diaminohexane (cas# 51857-17-1) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Formula: C₁₁H₂₄N₂O₂

Color and Shape: Neat

Molecular weight: 216.32

Ref: TR-B646500