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ChemicalBook > Product Catalogue >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >N-Boc-L-trans-4,5-Methanoproline

N-Boc-L-trans-4,5-Methanoproline

N-Boc-L-trans-4,5-Methanoproline Structure
  • ₹0
  • Product name: N-Boc-L-trans-4,5-Methanoproline
  • CAS: 197142-34-0
  • MF: C11H17NO4
  • MW: 227.26
  • EINECS:815-186-6
  • MDL Number:MFCD08691405
  • Synonyms:N-Boc-L-trans-4,5-Methanoproline;(1R,3S,5R)-2-[(tert-Butoxy)carbonyl]-2-azabicyclo[3.1.0]hexane-3-carboxyl+;N-Boc-L-trans-2-azabicyclo[3.1.0]hexane-3-carboxylic acid;2-Azabicyclo[3.1.0]hexane-2,3-dicarboxylic acid, 2-(1,1-dimethylethyl) ester, (1R,3S,5R)-;EOS-61213;(1R,3S,5R)-2-(tert-butoxyCARBONYL)-2-AZABICLO[3.1.0]hexane-3-carboxylic acid;(1R,3S,5R)-2-Boc-2-azabicyclo[3.1.0]hexane-3-carboxylic Acid;N-tert-butoxycarbonyl-l-trans-2-azabicyclo 3.1.0 hexane-3-carboxylic acid
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Boiling point :355.9±25.0 °C(Predicted)
Density :1.276±0.06 g/cm3(Predicted)
storage temp. :2-8°C
solubility :Acetone (Slightly, Sonicated), DMSO (Slightly, Sonicated), Methanol (Slightly, Heated)
pka :4.03±0.20(Predicted)
form :Solid
color :White to Pale Yellow
Stability :Hygroscopic

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

1R,3S,5R)-2-(tert-Butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic Acid acts as a reagent in the preparation of fused bicycles end-capped with peptide derivatives as HCV inhibitors. Synthesis of (tert-butoxycarbonyl)azabicyclohexanecarboxylic acid via stereoselective cyclopropanation of pyrroline

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