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Benzene, [[(1E)-1-ethenyl-1-heptenyl]sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136339-28-1

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136339-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136339-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,3 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 136339-28:
(8*1)+(7*3)+(6*6)+(5*3)+(4*3)+(3*9)+(2*2)+(1*8)=131
131 % 10 = 1
So 136339-28-1 is a valid CAS Registry Number.

136339-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name nona-1,3-dien-3-ylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names trans-(nona-1,3-diene-3-sulfonyl)-benzene

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:136339-28-1 SDS

136339-28-1Downstream Products

136339-28-1Relevant academic research and scientific papers

Stereoselective synthesis and reactivity of dienyl zirconocene derivatives

Chinkov, Nicka,Majumdar, Swapan,Marek, Ilan

, p. 2411 - 2417 (2007/10/03)

Stereoselective dienyl zirconocene derivatives have been prepared via a tandem allylic C-H bond activation isomerization-elimination reaction. These reagents can be either trapped directly with electrophiles or transmetalated to copper to participate in s

Stereoselective Preparation of Dienyl Zirconocene Complexes via a Tandem Allylic C-H Bond Activation-Elimination Sequence

Chinkov, Nicka,Majumdar, Swapan,Marek, Ilan

, p. 13258 - 13264 (2007/10/03)

Several dienyl zirconocene derivatives were easily prepared, as unique geometrical isomers, from simple non-conjugated unsaturated enol ethers with (1-butene)ZrCp2 complexes. This new methodology is based on a tandem allylic C-H bond activation-elimination sequence and the mechanism has been mapped out by deuterium labeling experiments. The stereochemical outcome of this process was determined by addition of several electrophiles. Moreover, when the organometallic derivative is vinylic as well as allylic such as in 44-47Zr, an unexpected reversal of the stereochemistry has been found during the zirconium to copper transmetalation step.

New approach to the stereoselective synthesis of metalated dienes via an isomerization-elimination sequence

Chinkov, Nicka,Majumdar, Swapan,Marek, Ilan

, p. 10282 - 10283 (2007/10/03)

Treatment of Cp2ZrBu2 with enol ether containing a remote double bond lead to conjugated metalated diene as single isomer via a tandem isomerization-elimination sequence. 2-Arylsulfonyl 1,3-dienes can also be used as a source of dienyl zirconocene derivatives, and the stereochemistry of the diene is dependent on the transmetalation reaction. Copyright

Radical cyclizations of functionalized allenes

Crandall,Ayers

, p. 3659 - 3662 (2007/10/02)

Substitution of P(O)Ph2, SOPh, and SO2Ph on an allene facilitates intramolecular radical addition to the central allene carbon to provide good yields of five-, six-, and seven-membered carbocycles.

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