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339267-24-2

339267-24-2

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339267-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 339267-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,2,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 339267-24:
(8*3)+(7*3)+(6*9)+(5*2)+(4*6)+(3*7)+(2*2)+(1*4)=162
162 % 10 = 2
So 339267-24-2 is a valid CAS Registry Number.

339267-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-N-methoxymethyl-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names -

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:339267-24-2 SDS

339267-24-2Downstream Products

339267-24-2Relevant articles and documents

Synthesis of trisphaeridine and norchelerythrine through palladium-catalyzed aryl-aryl coupling reactions

Harayama, Takashi,Akamatsu, Hisashi,Okamura, Kana,Miyagoe, Taeko,Akiyama, Toshihiko,Abe, Hitoshi,Takeuchi, Yasuo

, p. 523 - 528 (2007/10/03)

The synthesis of triphaeridine and norchelerythrine through palladium-catalyzed aryl-aryl coupling reactions was studied. The secondary amides were synthesized from 6-bromopiperonylicacid and aniline, and from piperonylic acid and 2-iodoaniline respectively, and were methoxymethylated for the preparation of starting materials for the cyclization reaction. All experiments were carried out in an argon atmosphere and the extract was washed with brine. The nuclear magnetic resonance (NMR) spectral data showed the presence of singlet signals due to aromatic proton in the products.

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