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3412-44-0

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3412-44-0 Usage

Synthesis Reference(s)

Tetrahedron Letters, 21, p. 27, 1980 DOI: 10.1016/S0040-4039(00)93615-3The Journal of Organic Chemistry, 31, p. 396, 1966 DOI: 10.1021/jo01340a012

Check Digit Verification of cas no

The CAS Registry Mumber 3412-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3412-44:
(6*3)+(5*4)+(4*1)+(3*2)+(2*4)+(1*4)=60
60 % 10 = 0
So 3412-44-0 is a valid CAS Registry Number.

3412-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-β-benzylstyrene

1.2 Other means of identification

Product number -
Other names 1,3-diphenylpropene

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:3412-44-0 SDS

3412-44-0Relevant articles and documents

Shapiro

, p. 345 (1968)

Nickel-Catalyzed C-Br/C-H Bis-phenylation of Methyl 4-Bromocrotonate: A Stereoselective Entry to Methyl (E)-3,4-Diphenylbut-2-enoate

Funicello, Maria,Chiummiento, Lucia,Lupattelli, Paolo,Tramutola, Francesco

, p. 1799 - 1806 (2015)

A method for C-Br/C-H bis-phenylation of methyl 4-bromocrotonate via nickel-catalyzed cross-coupling reaction has been developed. This protocol involves commercially available catalyst components and furnishes a suitable doubly phenylated building block.

Vinylation of Benzylic Amines via C-N Bond Functionalization of Benzylic Pyridinium Salts

Guan, Weiye,Liao, Jennie,Watson, Mary P.

, p. 3231 - 3237 (2018)

Cross-couplings of benzylic pyridinium salts and vinylboronic acids or esters have been developed. Via benzylic pyridinium intermediates, benzylic amines can be engaged in these cross-couplings through C-N bond functionalization. This method boasts mild reaction conditions and excellent tolerance for heteroaryl substituents and a range of functional groups.

Palladacycle-Catalyzed Regioselective Heck Reaction Using Diaryliodonium Triflates and Aryl Iodides

Hou, Cheng,Lei, Lu,Liang, Cui,Mo, Dong-Liang,Wang, Zhi-Xin,Zou, Pei-Sen

supporting information, p. 663 - 667 (2022/01/28)

We describe a P-containing palladacycle-catalyzed regioselective Heck reaction of 2,3-dihydrofuran with diaryliodonium salts and aryl iodides to afford 2-aryl-2,5-dihydrofurans and 2-aryl-2,3-dihydrofurans, respectively, in good yields. Mechanistic studie

Pd-Catalyzed Nazarov-Type Cyclization: Application in the Total Synthesis of β-Diasarone and Other Complex Cyclopentanoids

Bankar, Siddheshwar K.,Ramasastry, S. S. V.,Singh, Bara

supporting information, (2022/02/05)

We describe the palladium-catalyzed Nazarov-type cyclization of easily accessible (hetero)arylallyl acetates to pentannulated (hetero)arenes. This method provides ready access to various types of bi-, tri-, tetra-, and pentacyclic cyclopentanoids under ne

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