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tert-Butyl carbamate

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CAS:4248-19-5
Purity:99% Package:25KG
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CAS:4248-19-5
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CAS:4248-19-5
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CAS:4248-19-5
Purity:99% Package:25KG;5KG;1KG
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tert-Butyl carbamate manufacturers

  • tert-Butyl carbamate
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  • $50.00 / 1KG
  • 2024-04-26
  • CAS:4248-19-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 5MT per month
  • tert-Butyl carbamate
  • tert-Butyl carbamate pictures
  • $0.00 / 25KG
  • 2023-10-12
  • CAS:4248-19-5
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50000KG/month
  • tert-Butyl carbamate
  • tert-Butyl carbamate pictures
  • $50.00 / 1kg
  • 2023-09-08
  • CAS:4248-19-5
  • Min. Order: 1kg
  • Purity: 0.99
  • Supply Ability: 10000
tert-Butyl carbamate Basic information
Product Name:tert-Butyl carbamate
Synonyms:tert-Butylcarbamate,98+%;tert-Butoxycarbonylamine;Carbamic Acid tert-Butyl EsterBoc-amide;tert-Butyl carbamate,Boc-amide;Boc-NH2 N-t-Butoxycarbonyl-aMide;tert-Butyl carbaMate 5GR;tert-Butyl carbamate≥ 98%(GC);tert-Butyl carbaMate 98%
CAS:4248-19-5
MF:C5H11NO2
MW:117.15
EINECS:224-209-3
Product Categories:Protected Amino Acids;pharmacetical
Mol File:4248-19-5.mol
tert-Butyl carbamate Structure
tert-Butyl carbamate Chemical Properties
Melting point 105-108 °C (lit.)
Boiling point 218.95°C (rough estimate)
density 1.1274 (rough estimate)
refractive index 1.4206 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Needles
pka13.59±0.50(Predicted)
color White to slightly yellow
Water Solubility Soluble in methylene chloride, chloroform, and alcohols. Slightly soluble in petroleum ether and water.
BRN 1744500
CAS DataBase Reference4248-19-5(CAS DataBase Reference)
NIST Chemistry ReferenceTert-butyl carbamate(4248-19-5)
Safety Information
Hazard Codes Xi
Risk Statements 36
Safety Statements 39-26-24/25
WGK Germany 3
HS Code 29241990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
tert-Butyl carbamate Usage And Synthesis
Chemical PropertiesWhite to slightly yellow needles
Usestert-Butyl carbamate was used in palladium-catalyzed synthesis of N-Boc-protected anilines. It was used in the synthesis of tetrasubstituted pyrroles, functionalized with ester or ketone groups at C-3 position.
Synthesis Reference(s)The Journal of Organic Chemistry, 28, p. 3421, 1963 DOI: 10.1021/jo01047a033
General DescriptionPalladium-catalyzed cross-coupling reaction of tert-butyl carbamate with various aryl(Het) halides with Cs2CO3 as base in 1,4-dioxane (solvent) has been investigated.
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