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108233-82-5

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108233-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108233-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108233-82:
(8*1)+(7*0)+(6*8)+(5*2)+(4*3)+(3*3)+(2*8)+(1*2)=105
105 % 10 = 5
So 108233-82-5 is a valid CAS Registry Number.

108233-82-5SDS

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 prop-2-enyl 2-prop-2-enylhexanoate

1.2 Other means of identification

Product number -
Other names allyl 2-allylhexenoate

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:108233-82-5 SDS

108233-82-5Upstream product

108233-82-5Downstream Products

108233-82-5Relevant articles and documents

Palladium-Catalyzed Decarboxylation-Allylation of Allylic Esters of α-Substituted β-Keto Carboxylic, Malonic, Cyanoacetic, and Nitroacetic Acids

Tsuji, Jiro,,Yamada, Toshiro,Minami, Ichiro,Yuhara, Masami,Nisar, Mohammad,Shimizu, Isao

, p. 2988 - 2995 (2007/10/02)

Decarboxylation-allylation of allylic β-keto carboxylates using Pd(OAc)2-PPh3 or Pd2(dba)3*CHCl3-dppe as a catalyst proceeds smoothly to give α-allylated ketones.The reaction is highly regioselective.In some cases, diallylated ketones are obtained with allylic esters bearing an active proton(s).Also rhodium, molybdenum, and nickel complexes sre active catalysts in this reaction.Similarly allylic esters of α-substituted malonates, cyanoacetates, and nitroacetate undergo the palladium-catalyzed decarboxylation-allylation to afford allylated acetate, acetonitrile, and nitromethane, respectively.The mechanisms of these palladium-cataly zed decarboxylation-allylations are discussed

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