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Benzoyl chloride, 2-iodo-4,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113258-92-7

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113258-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113258-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,5 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 113258-92:
(8*1)+(7*1)+(6*3)+(5*2)+(4*5)+(3*8)+(2*9)+(1*2)=107
107 % 10 = 7
So 113258-92-7 is a valid CAS Registry Number.

113258-92-7SDS

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 2-iodo-4,5-dimethoxybenzoyl chloride

1.2 Other means of identification

Product number -
Other names Benzoyl chloride,2-iodo-4,5-dimethoxy

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:113258-92-7 SDS

113258-92-7Relevant academic research and scientific papers

Palladium-catalyzed tandem reaction to construct benzo[c]phenanthridine: Application to the total synthesis of benzo[c]phenanthridine alkaloids

Lv, Pei,Huang, Kanglun,Xie, Longguan,Xu, Xiaohua

, p. 3133 - 3135 (2011/05/15)

A concise and efficient synthesis of benzo[c]phenanthridines was accomplished by the palladium-catalyzed ring-opening coupling of azabicyclic alkene with o-iodobenzoates, followed by tandem cyclization. The strategy was successfully applied in the total synthesis of benzo[c]phenanthridine alkaloids such as sanguinarine, chelerythrine, nitidine and avicine.

A new and practical PIFA-promoted olefin amidohydroxylation: Six- versus five-membered ring formation

Serna, Sonia,Tellitu, Imanol,Domínguez, Esther,Moreno, Isabel,SanMartín, Raúl

, p. 3483 - 3486 (2007/10/03)

A novel access to the isoindolinone and isoquinolin-2-one skeletons from adequately substituted aromatic precursors is described. The key intramolecular cyclization step was performed by the action of phenyliodine(III)bis(trifluoroacetate) (PIFA) on the c

Concise synthesis of nitidine by palladium-assisted biaryl coupling reaction

Harayama, Takashi,Shibaike, Kentaro

, p. 191 - 195 (2007/10/03)

Formal total synthesis of nitidine (1) was accomplished via oxynitidine (7) by the internal aryl-aryl coupling reaction of iodo-amide (6) using palladium-assisted cyclization reaction.

Biphenyl derivatives, process for preparing the same and intermediates therefor

-

, (2008/06/13)

Novel biphenyl derivatives of the formula: wherein R1 is a substituted or unsubstituted aminocarbonyl group, aminothiocarbonyl group, a substituted or unsubstituted lower alkoxycarbonyl group, cyano group, or a group of the formula: STR1 one or

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