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Benzene, 1-(2-butenyl)-2-methyl-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34136-21-5

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34136-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34136-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,3 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34136-21:
(7*3)+(6*4)+(5*1)+(4*3)+(3*6)+(2*2)+(1*1)=85
85 % 10 = 5
So 34136-21-5 is a valid CAS Registry Number.

34136-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1-(but-2-en-1-yl)-2-methylbenzene

1.2 Other means of identification

Product number -
Other names (Z)-2-Methyl-(2-butenyl)benzol

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:34136-21-5 SDS

34136-21-5Downstream Products

34136-21-5Relevant academic research and scientific papers

Ligandless iron-catalyzed desulfinylative C-C allylation reactions using Grignard reagents and alk-2-enesulfonyl chlorides

Volla, Chandra M. R.,Markovic, Dean,Dubbaka, Srinivas Reddy,Vogel, Pierre

scheme or table, p. 6281 - 6288 (2011/02/28)

Alk-2-enesulfonyl chlorides 1-4 were synthesized by the BCl3-promoted ene reaction of alkenes with SO2. These sulfonyl chlorides were then used as electrophilic partners in iron-catalyzed desulfinylative cross-coupling reactions with different Grignard reagents (aromatic, aliphatic, and heteroaromatic). The reaction can be catalyzed with even 2 mol-% of the simple iron salt Fe(acac)3. The regioselectivity of these allylations was studied by using sulfonyl chlorides 3 and 4 with aryl Grignard reagents. The scope of these allylations was further extended by the coupling of ester-substituted alk-2-enesulfonyl chloride 10 with aromatic Grignard reagents. Symmetrical products were synthesized by double C-C allylation with the use of 2-methylidenepropane-1,3-disulfonyl chloride (12). Wiley-VCH Verlag GmbH & Co. KGaA.

Hydrogen peroxide-or sodium hypochlorite-induced bromination of 1-arylbut-2-enes

Sadygov,Alimardanov

, p. 1661 - 1670 (2008/09/18)

Bromination of 1-arylbut-2-enes in the system [HBr or NaBr (KBr)-HX]-H 2O2 (or NaOCl) under relatively mild conditions leads to electrophilic addition of bromine or hypobromous acid at the side-chain double bond. Under more severe conditions, the process is accompanied by bromination of the aromatic ring. Treatment of the title compounds with peroxy acids (RCOOH-H2O2) gives the corresponding epoxy derivatives which react with HBr and oxygen-containing nucleophiles to produce α-bromo alcohols, diols, and diol acetates.

REGIO- AND STEREO-CHEMISTRY IN ALLYLATION OF ARYL GRINARD REAGENTS CATALYZED BY PHOSPHINE-NICKEL AND -PALLADIUM COMPLEXES

Hayashi, Tamio,Konishi, Mitsuo,Yokota, Kan-Ichi,Kumada, Makoto

, p. 359 - 374 (2007/10/02)

Nickel and palladium complexes with the 1,1'-bis(diphenylphosphino)ferrocene ligand effectively catalyze regioselective cross-coupling of allylic ethers such as 1- or 3-methyl-2-propenyl silyl ethers with aryl-Grinard reagents, where the nickel catalyst l

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