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Benzene, 1,3-dimethyl-5-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14646-21-0

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14646-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14646-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,4 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14646-21:
(7*1)+(6*4)+(5*6)+(4*4)+(3*6)+(2*2)+(1*1)=100
100 % 10 = 0
So 14646-21-0 is a valid CAS Registry Number.

14646-21-0SDS

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 1,3-dimethyl-5-prop-1-en-2-ylbenzene

1.2 Other means of identification

Product number -
Other names 1-Isopropenyl-3,5-dimethylbenzol

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:14646-21-0 SDS

14646-21-0Relevant academic research and scientific papers

Formal Allylation and Enantioselective Cyclopropanation of Donor/Acceptor Rhodium(II) Azavinyl Carbenes

Liu, Zhili,Chen, Lianfen,Zhu, Dong,Zhu, Shifa

supporting information, p. 1275 - 1279 (2021/02/20)

A highly efficient formal allylation of dihydronaphthotriazoles with alkenes under rhodium(II) catalysis is reported. Various allyl dihydronaphthalene derivatives were furnished via rhodium(II) azavinyl carbenes with moderate to good yields and excellent chemoselectivity. When monosubstituted alkenes are used, cyclopropanation occurs and good to excellent enantioselectivities have been achieved. Particularly noteworthy is the allylic C(sp2)-H activation instead of traditional C(sp3)-H activation in the formal allylation process.

Electrochemical oxidative radical oxysulfuration of styrene derivatives with thiols and nucleophilic oxygen sources

Wang, Yang,Deng, Lingling,Mei, Haibo,Du, Bingnan,Han, Jianlin,Pan, Yi

supporting information, p. 3444 - 3449 (2018/08/06)

Oxydifunctionalization of olefins represents a powerful tool and yet poses a challenging task. Previous methods have usually required a stoichiometric amount of a strong oxidant and an expensive transition-metal catalyst. This work describes the first example of the electrochemical oxysulfuration reaction of olefins with thiols and nucleophilic oxygen sources. This electrochemical difunctionalization reaction is conducted under catalyst- and oxidant-free conditions, and shows good substrate generality, affording thio-substituted alcohols, ethers and γ-lactones in good chemical yields and with excellent regioselectivities. This work represents a new and green strategy for the difunctionalization of olefins, and also provides a complementary and highly valuable prospect for current methodologies for the synthesis of thio-substituted compounds.

A Metal-Free Oxidative Dehydrogenative Diels–Alder Reaction for Selective Functionalization of Alkylbenzenes

Manna, Srimanta,Antonchick, Andrey P.

supporting information, p. 7825 - 7829 (2017/06/06)

Functionalization of C(sp3)?H bonds under metal-free reaction conditions is a great challenge due to poor bond reactivity. A novel metal-free oxidative dehydrogenative Diels–Alder reaction of alkylbenzene derivatives with alkenes through C(sp3)?H bond functionalization is described. The developed oxidative method provides a straightforward approach to biologically relevant 1,4-phenanthraquinone and isoindole derivatives from readily available starting materials. Furthermore, the synthesis of nitrostyrenes from enylbenzene derivatives by selective C(sp3)?H bond functionalization has been demonstrated.

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