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METHOXYALLENE; 95%DISCONTINUED 05/24/01

METHOXYALLENE; 95%DISCONTINUED  05/24/01 Structure
  • ₹3450 - ₹11430
  • Product name: METHOXYALLENE; 95%DISCONTINUED 05/24/01
  • CAS: 13169-00-1
  • MF: C4H6O
  • MW: 70.09
  • EINECS:
  • MDL Number:MFCD00153022
  • Synonyms:Propadienylmethyl ether;Allenyl methyl ether;1-Methoxypropa-1,2-diene;NSC 363923;Methoxyallene technical grade;95%DISCONTINUED 05/24/01;METHOXYALLENE; 95%DISCONTINUED 05/24/01;1,2-Propadiene, 1-methoxy-
2 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 1G
  • 5G
  • ManufacturerSigma-Aldrich(India)
  • Product number694126
  • Product descriptionMethoxyallene technical grade
  • Packaging1G
  • Price₹3450
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number694126
  • Product descriptionMethoxyallene technical grade
  • Packaging5G
  • Price₹11430
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 694126 Methoxyallene technical grade 1G ₹3450 2022-06-14 Buy
Sigma-Aldrich(India) 694126 Methoxyallene technical grade 5G ₹11430 2022-06-14 Buy

Properties

Boiling point :48.2℃ (760 torr)
Density :0.832 g/mL at 25 °C
refractive index :n20/D 1.429
Flash point :-29 °C
storage temp. :2-8°C

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Danger
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H225 Highly Flammable liquid and vapour Flammable liquids Category 2 Danger GHS hazard pictograms P210,P233, P240, P241, P242, P243,P280, P303+ P361+P353, P370+P378,P403+P235, P501
Precautionary statements:
P210 Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

Description

Reactant involved in:• ;Multicomponent reactions with nitriles and carboxylic acids followed by cyclocondensation for synthesis of enantiopure pyridines1• ;Intermolecular hydroamination2• ;One-pot synthesis of alkoxy and (alkylsulfanyl)-substituted pyrroles and dihydropyridines3• ;Intermolecular [4+2] cycloaddition with dienes4• ;Allenyl cyclization and subsequent transformation into dicarbonyl, cyclopentenones, and butenolide compounds5• ;Insertion reactions of C-C pi-bonds into alkylidenesilacyclopropanes6

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