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Propanedioic acid, methyl(2-phenoxy-2-propenyl)-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403855-58-3

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403855-58-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403855-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,8,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 403855-58:
(8*4)+(7*0)+(6*3)+(5*8)+(4*5)+(3*5)+(2*5)+(1*8)=143
143 % 10 = 3
So 403855-58-3 is a valid CAS Registry Number.

403855-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-methyl-2-(2-phenoxyprop-2-enyl)propanedioate

1.2 Other means of identification

Product number -
Other names methyl 2-(methylcarboxy)-2-methyl-4-phenoxypent-4-enoate

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:403855-58-3 SDS

403855-58-3Downstream Products

403855-58-3Relevant academic research and scientific papers

On the regiochemistry of nucleophilic attack on 2-halo π-allyl complexes. 4. The effect of silver acetate and nucleophile concentrations in competitive nucleophilic attack with malonate and phenoxide nucleophiles

Organ, Michael G.,Arvanitis, Elena A.,Hynes, Stephen J.

, p. 3918 - 3922 (2007/10/03)

2,3-Dibromo-l-propene or its allyl carbonate analogue are ionized under Pd catalysis to generate the 2-bromo Pd-π-allyl complex (triphenylphosphine ligand), which alkylates with malonate nucleophile at the terminal position. The presence of acetate ion in

Controlling chemoselectivity in vinyl and allylic C-X bond activation with palladium catalysis: A pKa-based electronic switch

Organ, Michael G.,Arvanitis, Elena A.,Dixon, Craig E.,Cooper, Jeremy T.

, p. 1288 - 1294 (2007/10/03)

It has been demonstrated that the same Pd catalyst can be used to effect allylic substitution or vinylic cross-coupling reactions selectively and interchangeably on polyfunctionalized olefin building blocks despite the differences in reaction mechanism. T

On the regiochemistry of nucleophilic attack on 2-halo π-allyl complexes. Part 3: The electronic effect of phenoxide ion and the ligand

Organ, Michael G.,Arvanitis, Elena A.,Hynes, Stephen J.

, p. 8989 - 8992 (2007/10/03)

2,3-Dibromo-1-propene was subjected to competitive attack by malonate and different phenoxide nucleophiles in the presence of Pd substituted with monodentate or bidentate ligands. The presence of phenoxide promotes central carbon attack on the initially-f

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