Welcome to LookChem.com Sign In|Join Free
  • or
(3-methoxyphenyl)methyl methyl carbonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1350846-02-4

Post Buying Request

1350846-02-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1350846-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1350846-02-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,0,8,4 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1350846-02:
(9*1)+(8*3)+(7*5)+(6*0)+(5*8)+(4*4)+(3*6)+(2*0)+(1*2)=144
144 % 10 = 4
So 1350846-02-4 is a valid CAS Registry Number.

1350846-02-4Relevant academic research and scientific papers

Palladium-catalyzed benzylic substitution of benzyl carbonates with phosphorus nucleophiles

Makida, Yusuke,Usui, Kazumi,Ueno, Satoshi,Kuwano, Ryoichi

supporting information, p. 1814 - 1817 (2017/11/23)

A wide range of benzyl carbonates reacted with dimethyl phosphonate or diphenylphosphine oxide in the presence of the palladium catalyst, [Pd(η3-allyl)Cl]2DPEphos, to give dimethyl benzylphosphonates and benzyldiphenylphosphine oxides in high yields. The catalytic phosphonylation was applied to the one-pot synthesis of alkenes from the benzyl esters.

A general Pd-catalyzed α- And γ-benzylation of aldehydes for the formation of quaternary centers

Franzoni, Ivan,Guénée, Laure,Mazet, Clément

supporting information, p. 6338 - 6343 (2015/06/08)

A palladium-catalyzed benzylation of α-branched aldehydes has been developed using benzyl methyl carbonates. The method gives access to congested quaternary centers in the vicinity of one of the most sensitive carbonyl functionalities and displays unprecedented generality with respect to both coupling partners. Evidence for the direct involvement of a Pd-η3-benzyl intermediate is provided. Extension of this strategy to the γ-benzylation of α,β-unsaturated aldehydes is further demonstrated.

Palladium-catalyzed C3-benzylation of indoles

Zhu, Ye,Rawal, Viresh H.

supporting information; experimental part, p. 111 - 114 (2012/03/07)

A general method for regioselective C3-benzylation of indoles has been developed. Various 3-substituted indoles and benzyl methyl carbonates with different electronic properties react under mild conditions to afford a diverse range of 3-benzylindolenine products in good yields.

Intramolecular SN′-type aromatic substitution of benzylic carbonates at their para-position

Ueno, Satoshi,Komiya, Sadakazu,Tanaka, Takeshi,Kuwano, Ryoichi

supporting information; experimental part, p. 338 - 341 (2012/03/10)

The benzylic carbonates, which connect with an active methine through an o-phenylene tether at their meta-position, are cyclized by Pd(η3- C3H5)Cp-S-Phos catalyst, yielding 3-methyl-9,10- dihydrophenanthrenes. In the catal

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1350846-02-4