CAS 68076-36-8
:N-boc-1,4-diaminobutane
Description:
N-Boc-1,4-diaminobutane, with the CAS number 68076-36-8, is a chemical compound characterized by the presence of a butane backbone with two amine functional groups at the 1 and 4 positions, and a tert-butyloxycarbonyl (Boc) protecting group attached to one of the amines. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other nitrogen-containing compounds, due to its ability to protect amine functionalities during chemical reactions. N-Boc-1,4-diaminobutane is generally a solid at room temperature and is soluble in polar organic solvents. Its structure allows for the introduction of various functional groups, making it versatile in synthetic chemistry. The Boc group can be removed under mild acidic conditions, regenerating the free amine for further reactions. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper laboratory practices are followed.
Formula:C9H20N2O2
InChI:InChI=1/C9H20N2O2/c1-9(2,3)13-8(12)11-7-5-4-6-10/h4-7,10H2,1-3H3,(H,11,12)/p+1
Synonyms:- N-(4-Aminobutyl)carbamic acid tert-butyl ester
- N-Boc-1,4-butanediamine
- Tert-Butyl (4-Aminobutyl)Carbamate
- 4-[(Tert-Butoxycarbonyl)Amino]Butan-1-Aminium
- Tert-Butyl 4-Aminobutylcarbamate
- tert-Butyl N-(4-aminobutyl)carbamate
- N-1-BOC-1,4-DIAMINOBUTANE HCL
- (4-AMINOBUTYL)CARBAMIC ACID E-TERT-BUTYL ESTER HYDROCHLORIDE
- BOC-DIAMINOBUTANE HCL
- N-T-BUTYLOXYCARBONYL-1,4-DIAMINOBUTANE HYDROCHLORIDE
- 1-BOC-AMINO-1,4-BUTANEDIAMINE
- BUTTPARK 121\06-09
- N-BOC-1,4-DIAMINOBUTANE HYDROCHLORIDE
- BOC-NH(CH2)4NH2 HCL
- N-BOC-1,4-DIAMINOBUTANE
- BOC-DAB HCL
- N-(TERT-BUTOXYCARBONYL)-1,4-DIAMINOBUTANE
- N-T-BOC-BUTANDIAMINE HCL
- N-(TERT-BUTOXYCARBONYL)-1,4-BUTANEDIAMINE
- AURORA KA-4397
- BOC-1,4-DIAMINOBUTANE HCL
- MONO-4-N-BOC-1,4-DIAMINOBUTANE
- N-1-T-BUTOXYCARBONYL-1,4-DIAMINOBUTANE HYDROCHLORIDE
- See more synonyms
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Found 10 products.
N-(tert-Butoxycarbonyl)-1,4-diaminobutane
CAS:Formula:C9H20N2O2Purity:>98.0%(GC)(T)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:188.27N-Boc-1,4-diaminobutane, 97+%
CAS:<p>N-Boc-1,4-diaminobutane is used in preparation of pharmacologically active compounds, preparation of spermidine analogues and in introduction of a C4-spacer. It serve as intermediates of medicine. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfoli</p>Formula:C9H21N2O2Purity:97+%Color and Shape:Colorless to yellow, LiquidMolecular weight:189.28tert-Butyl N-(4-aminobutyl)carbamate
CAS:Formula:C9H20N2O2Purity:98%Color and Shape:LiquidMolecular weight:188.2673tert-Butyl N-(4-aminobutyl)carbamate
CAS:<p>tert-Butyl N-(4-aminobutyl)carbamate</p>Formula:C9H20N2O2Purity:97%Color and Shape: colourless liquidMolecular weight:188.27g/mol1-Boc-1,4-butanediamine
CAS:Formula:C9H20N2O2Purity:98.0%Color and Shape:Liquid, ViscousMolecular weight:188.271NH2-C4-NH-Boc
CAS:<p>NH2-C4-NH-Boc (compound 15) is a PROTAC linker belonging to the Alkyl/ether class. NH2-C4-NH-Boc can be used to synthesize a series of PROTAC molecules.</p>Formula:C9H20N2O2Purity:99.90%Color and Shape:SolidMolecular weight:188.274-Aminobutylcarbamic Acid tert-Butyl Ester
CAS:Controlled Product<p>Applications 4-Aminobutylcarbamic Acid tert-Butyl Ester is used in the synthesis of iron chelators expressing antitumor activity. Also used in the synthesis of iron oxide nanoparticles which are used in cellular and small animal imaging.<br>References Corce, V. et al.: Bioconj. Chem., 25, 320 (2014); Stanicki, D. et al., J. mat. Chem. B. Mat. Biol. Med.: 2, 387 (2014);<br></p>Formula:C9H20N2O2Color and Shape:NeatMolecular weight:188.27N-(tert-Butoxycarbonyl)-1,4-diaminobutane
CAS:<p>N-(tert-Butoxycarbonyl)-1,4-diaminobutane is a cationic polymer that is used for transfection. It has been shown to have high efficiency in the transfection of DNA into cells and polymers that are biodegradable and can be dissolved in water. This chemical compound also has an acidic pH range, which makes it useful for the treatment of intracellular environments with a low pH. N-(tert-Butoxycarbonyl)-1,4-diaminobutane has been shown to cause cytotoxicity in cells at high concentrations, but has no effects on cells at lower concentrations. The disulfide bonds of this compound make it endosomal-lytic and nonviral.</p>Formula:C9H20N2O2Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:188.27 g/mol4-Aminobutylcarbamic Acid tert-Butyl Ester-d3
CAS:Controlled ProductFormula:C9D3H17N2O2Color and Shape:NeatMolecular weight:191.286







