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35466-83-2

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35466-83-2 Usage

Chemical Properties

Clear colorless liquid

Uses

Employed in the Pd(0)-mediated synthesis of allyl aryl ethers and sulfides, and α,β-unsaturated carbonyls.

Check Digit Verification of cas no

The CAS Registry Mumber 35466-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,6 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35466-83:
(7*3)+(6*5)+(5*4)+(4*6)+(3*6)+(2*8)+(1*3)=132
132 % 10 = 2
So 35466-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O3/c1-3-4-8-5(6)7-2/h3H,1,4H2,2H3

35466-83-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Aldrich

  • (381381)  Allylmethylcarbonate  98%

  • 35466-83-2

  • 381381-5ML

  • 1,117.35CNY

  • Detail
  • Aldrich

  • (381381)  Allylmethylcarbonate  98%

  • 35466-83-2

  • 381381-25ML

  • 3,222.18CNY

  • Detail

35466-83-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl prop-2-enyl carbonate

1.2 Other means of identification

Product number -
Other names allyl-OC(O)OMe

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35466-83-2 SDS

35466-83-2Relevant articles and documents

Synthesis of Carbonate Esters by Carboxymethylation Using NaAlO2 as a Highly Active Heterogeneous Catalyst

Ramesh, Sreerangappa,Indukuri, Kiran,Riant, Olivier,Debecker, Damien P.

, p. 1846 - 1851 (2019/01/04)

Sodium aluminate is presented as a highly active heterogeneous catalyst that is able to convert a range of alcohols into the corresponding unsymmetrical carbonate esters by reaction with dimethyl carbonate. Preparing NaAlO2 via spray drying boosts the basic properties and the activity of the catalyst.

Rate and product studies on the solvolyses of allyl chloroformate

Koh, Han Joong,Kang, Suk Jin

, p. 4117 - 4121 (2013/08/23)

The solvolysis rate constants of allyl chloroformate (CH 2=CHCH2OCOCl, 3) in 30 different solvents are well correlated with the extended Grunwald-Winstein equation, using the NT solvent nucleophilicity scale and YCl solvent ionizing scale, with the sensitivity values of 0.93 ± 0.05 and 0.41 ± 0.02 for l and m, respectively. These l and m values can be considered to support a S N2 reaction pathway. The activation enthalpies (ΔH≠) were 12.5 to 13.4 kcal·mol-1 and the activation entropies (ΔS≠) were -34.4 to -37.3 cal·mol-1·K -1, which is also consistent with the proposed bimolecular reaction mechanism. The solvent kinetic isotope effect (SKIE, kMeOH/k MeOD) of 2.16 was also in accord with the SN2 mechanism. The values of product selectivity (S) for the solvolyses of 3 in alcohol/water mixtures was 1.3 to 3.9, which is also consistent with the proposed bimolecular reaction mechanism.

ETHYLENICALLY UNSATURATED MONOMERS COMPRISING ALIPHATIC AND AROMATIC MOIETIES

-

Page/Page column 35-38, (2009/10/22)

Polymerizable monomers comprising at least one 1- or 2-propylene moiety and further comprising both aromatic moieties and additional aliphatic moieties and polymerizable mixtures, resins and thermoset products based on these monomers.

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