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17342-56-2

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17342-56-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17342-56-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,4 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17342-56:
(7*1)+(6*7)+(5*3)+(4*4)+(3*2)+(2*5)+(1*6)=102
102 % 10 = 2
So 17342-56-2 is a valid CAS Registry Number.

17342-56-2SDS

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 3-phenylbut-2-enylbenzene

1.2 Other means of identification

Product number -
Other names but-2-ene-1,3-diyldibenzene

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:17342-56-2 SDS

17342-56-2Downstream Products

17342-56-2Relevant articles and documents

REACTION OF PHENYL DERIVATIVES OF LANTHANIDES WITH CARBONYL COMPOUNDS

Sigalov, A. B.,Petrov, E. S.,Rybakova, L. F.,Beletskaya, I. P.

, p. 2351 - 2356 (1983)

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Iron-Catalyzed Highly Enantioselective Hydrogenation of Alkenes

Lu, Dongpo,Lu, Peng,Lu, Zhan,Ren, Xiang,Sun, Yufeng,Xu, Haofeng

supporting information, p. 12433 - 12438 (2021/08/23)

Here, we reported for the first time an iron-catalyzed highly enantioselective hydrogenation of minimally functionalized 1,1-disubstituted alkenes to access chiral alkanes with full conversion and excellent ee. A novel chiral 8-oxazoline iminoquinoline ligand and its iron complex have been designed and synthesized. This protocol is operationally simple by using 1 atm of hydrogen gas and shows good functional group tolerance. A primary mechanism has been proposed by the deuterium-labeling experiments.

Nickel-Catalyzed Benzylation of Aryl Alkenes with Benzylamines via C-N Bond Activation

Yu, Hui,Hu, Bin,Huang, Hanmin

, p. 13922 - 13929 (2018/11/23)

We have developed the first example of nickel-catalyzed Heck-type benzylation of aryl olefins with various benzylamines as benzyl electrophiles, and the benzylic C-N bond cleavage was efficiently promoted by the amine-I2 charge transfer complex (CT complex). The combination of low-cost NiCl2 and I2 has been found to facilitate Heck reaction of tertiary benzylamines and alkenes into various benzyl-substituted alkenes in good to excellent yields. This unconventional Heck reaction is proposed to go through initially the formation of a benzylic radical via oxidative addition of the C-N bond with Ni(0), then capturing by aryl alkene via radical addition, followed by single-electron transfer redox and proton abstraction without oxidant and external base.

REACTIONS OF PHENYL DERIVATIVES OF LANTHANIDES WITH UNSATURATED KETONES

Sigalov, A. B.,Rybakova, L. F.,Beletskaya, I. P.

, p. 1539 (2007/10/02)

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