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2(1H)-Naphthalenone, 1,1-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74849-12-0

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74849-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74849-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,4 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74849-12:
(7*7)+(6*4)+(5*8)+(4*4)+(3*9)+(2*1)+(1*2)=160
160 % 10 = 0
So 74849-12-0 is a valid CAS Registry Number.

74849-12-0SDS

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 1,1-dibenzylnaphthalen-2-one

1.2 Other means of identification

Product number -
Other names 1,1-dibenzyl-1,2-dihydronaphthalen-2-one

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:74849-12-0 SDS

74849-12-0Relevant academic research and scientific papers

Influence of phase transfer catalyst structure on selectivity

Dehmlow, E. V.

, p. 1998 - 2005 (2007/10/03)

A concise review is given of systematic studies concerned with the tuning of regio-, "frequentio-", chemo-, and diastereoselectivity by the structure or type of phase transfer catalyst. - Keywords: phase transfer catalysis; regioselectivity; selectivity control; stereoselectivity; C/O-alkylation; C/N-alkylation.

Novel Rearrangement and Cyclization Processes Resulting from Bromination of 1,1-Dibenzyltetralin Derivatives

Miller, Bernard,Shi, Xiaolian

, p. 1677 - 1681 (2007/10/02)

Addition of bromine to hydrocarbon 1 results in an aromatic alkylation to form the bicyclononane derivative 5.Addition of bromine to ketone 3 in acetonitrile solution results in a dienone-phenol rearrangement to form phenol 6, while reaction of ket

HIGHLY SELECTIVE BENZILATIONS OF β-NAPHTHOXIDE ANION IN HETEROGENEOUS MEDIA

Bram, G.,Loupy, A.,Sansoulet, J.,Vaziri-Zand, F

, p. 5035 - 5038 (2007/10/02)

Each of the four products resulting from the benzylation of the ambident β-naphthoxide anion can be efficiently and selectively obtained in mild an economical conditions by a judicious choice of the solid base: LiOH, LiOtBu or KOH-Aliquat.

Regioselectivity of the Alkylation of Ambident Anionic Species on Alumina or in the Presence of 'Solid Hexamethylphosphoric Triamide'

Bram, Georges,Geraghty, Niall,Nee, Gerard,Seyden-Penne, Jacqueline

, p. 325 - 326 (2007/10/02)

C-Alkylation of the acetoacetate anions and of sodium naphthoxide is highly favoured on alumina, while O-alkylation of the acetoacetate anion predominates in tetrahydrofuran in the presence of solid hexamethylphosphoric triamide.

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