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Plumbane, tris(acetyloxy)(2,4-dimethoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36896-61-4

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36896-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36896-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,9 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36896-61:
(7*3)+(6*6)+(5*8)+(4*9)+(3*6)+(2*6)+(1*1)=164
164 % 10 = 4
So 36896-61-4 is a valid CAS Registry Number.

36896-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [diacetyloxy-(2,4-dimethoxyphenyl)plumbyl] acetate

1.2 Other means of identification

Product number -
Other names Plumbane,tris(acetyloxy)(2,4-dimethoxyphenyl)

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:36896-61-4 SDS

36896-61-4Relevant academic research and scientific papers

β-DIKETONE INTERACTIONS. Part 10. The structures and properties of 3-(2',4'-dimethoxyphenyl)pentane-2,4-dione; enol ring symmetry and other halogen bond parameters

Emsley, John,Ma, Lewina Y. Y.,Karaulov, Sacha A.,Motevalli, Majid,Hursthouse, Michael B.

, p. 143 - 152 (1990)

The X-ray crystal structure of the title compound shows it to be the enol tautomer and with two molecules in the unit cell, with hydrogen bond lengths, R(O..O=, of 2.446 and 2.474 Angstroem.These and other hydrogen bond parameters (δ, Δδ(H-D) and νOH

Enantioselective construction of sterically hindered tertiary α-aryl ketones: A catalytic asymmetric synthesis of isoflavanones

Carroll, Michael P.,Mueller-Bunz, Helge,Guiry, Patrick J.

supporting information, p. 11142 - 11144 (2013/01/15)

A method for the catalytic asymmetric α-arylation of ketones bearing very sterically hindered aryl rings has been developed. This reaction occurs under mild conditions, in short reaction times and has been applied to the first catalytic asymmetric synthesis of isoflavanones.

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