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N-[2-Chloro-3-formyl-4-pyridinyl]carbamic acid tert-butyl ester

N-[2-Chloro-3-formyl-4-pyridinyl]carbamic acid tert-butyl ester Structure
  • ₹0
  • Product name: N-[2-Chloro-3-formyl-4-pyridinyl]carbamic acid tert-butyl ester
  • CAS: 893423-62-6
  • MF: C11H13ClN2O3
  • MW: 256.69
  • EINECS:
  • MDL Number:MFCD16659013
  • Synonyms:4-(Boc-aMino)-2-chloro-3-pyridinecarbaldehyde;N-(2-chloro-3-forMyl-4-pyridinyl)carbaMic acid 1,1-diMethylethyl ester;ert-Butyl (2-chloro-3-forMylpyridin-4-yl)carbaMate;baMicacid,(2-chloro-3-forMyl-4-pyridinyl)-,1,1-;tert-Butyl N-(2-chloro-3-formyl-4-pyridyl)carbamate;tert-Butyl (2-chloro-3-formylpyridin-4-yl);N-[2-Chloro-3-formyl-4-pyridinyl]carbamic acid tert-butyl ester;CarbaMic acid, N-(2-chloro-3-forMyl-4-pyridinyl)-, 1,1-diMethylethyl ester
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Boiling point :332℃
Density :1.314
Flash point :155℃
storage temp. :under inert gas (nitrogen or Argon) at 2-8°C
pka :11.46±0.70(Predicted)
form :crystalline powder
color :White

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:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312 IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

4-(Boc-amino)-2-chloro-3-pyridinecarbaldehyde is used as a reagent in the synthesis of naphthyridinones as allosteric dual Akt1 and Akt2 inhibitors.

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