ChemicalBook Product Catalog Organic Chemistry Amides Amino compound tert-butyl (4-bromobutyl)carbamate

tert-butyl (4-bromobutyl)carbamate

tert-butyl (4-bromobutyl)carbamate Basic information
Product Name:tert-butyl (4-bromobutyl)carbamate
Synonyms:Carbamic acid,N-(4-bromobutyl)-, 1,1-dimethylethyl ester;N-(4-BroMobutyl)carbaMic Acid 1,1-DiMethylethyl Ester;N-(tert-Butoxycarbonyl)-1-broMobutan-4-ylaMine;N-Boc 4-broMobutan-1-aMine;tert-Butyl 4-bromobutylcarbamate;4-(Boc-aMino)butyl broMide technical, >=90% (AT);tert-Butyl (4-bromobutyl);ert-butylN-(4-bromobutyl)carbamate
CAS:164365-88-2
MF:C9H18BrNO2
MW:252.15
EINECS:200-158-5
Product Categories:Aliphatics;Bifunctional Crosslinkers;Building Blocks;Chemical Biology;Chemical Synthesis;Linkers;Nitrogen Compounds;Organic Building Blocks;Peptide Chemistry;Protected Amines
Mol File:164365-88-2.mol
tert-butyl (4-bromobutyl)carbamate Structure
tert-butyl (4-bromobutyl)carbamate Chemical Properties
Boiling point 308.8±25.0 °C(Predicted)
density 1.228
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Low-Melting Solid
pka12.76±0.46(Predicted)
color White to Pale Yellow
Safety Information
Hazard Codes Xi
Risk Statements 41
Safety Statements 26-39
WGK Germany 3
MSDS Information
tert-butyl (4-bromobutyl)carbamate Usage And Synthesis
Chemical PropertiesOff-White Low Melting Solid
Uses4-(Boc-amino)butyl bromide can be used:
  • For the synthesis of N-Boc-aminoalkoxyphenyl derivatives, precursor to pharmacophore elements for the treatment of glaucoma.
  • For the synthesis of various aloperine derivatives with potential application as anti-HIV agents.
  • For the modification of 4,5,6,7-tetrabromobenzotriazole (TBB) derivatives to generate improved CK2 inhibitors.
HEXAHYDRO-PYRROLO[3,4-B]PYRROLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester 7-AMINO-3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXYLIC ACID TERT-BUTYL ESTER Iodoform tert-butyl N-[3-[methoxy(methyl)amino]-3-oxopropyl]carbamate 3(S)-BROMOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 3(R)-BROMOMETHYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER tert-Butyl 3-(bromomethyl)pyrrolidine-1-carboxylate 3-BROMO-4-OXO-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 2-BROMO-2- (1-TERT-BUTOXYCARBONYL-PYRROLIDIN-3-YL)-MALONIC ACID DIMETHYL ESTER 1-N-BOC-3-BROMOPIPERIDINE 2-tert-Butyl 6-methyl 4-bromo-3-oxo-2-azabicyclo[3.1.0]hex-3-ene-2,6-dicarboxylate 2-BROMO-2- (1-TERT-BUTOXYCARBONYL-PIPERIDIN-4-YL)-MALONIC ACID DIMETHYL ESTER 4-Bromomethypiperidine-1-carboxylic acid tert-butyl ester 4-(BROMO-METHOXYCARBONYL-METHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER TERT-BUTYL 3-(2-BROMOETHYL)PIPERIDINE-1-CARBOXYLATE A-BROMO-1-[(1,1-DIMETHYLETHOXY)CARBONYL]-4-PIPERIDINEACETIC ACID (3-BROMO-4,5-DIHYDRO-ISOXAZOL-5-YLMETHYL)-CARBAMIC ACID TERT-BUTYL ESTER
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