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354574-31-5

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354574-31-5 Usage

General Description

Benzenamine, 2-iodo-6-methoxy- is a chemical compound with the molecular formula C7H8INO that is used in organic synthesis and medicinal chemistry. It is a substituted aniline, with a methyl group and a methoxy group attached to the benzene ring, as well as an iodine atom in the para position. Benzenamine, 2-iodo-6-methoxy- is a key building block in the synthesis of various pharmaceuticals and agrochemicals, and it is also used as a precursor in the preparation of dyes and other organic compounds. Its unique structure and reactivity make it a valuable starting material for the production of a wide range of useful products in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 354574-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,5,7 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 354574-31:
(8*3)+(7*5)+(6*4)+(5*5)+(4*7)+(3*4)+(2*3)+(1*1)=155
155 % 10 = 5
So 354574-31-5 is a valid CAS Registry Number.

354574-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-6-methoxyaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2-iodo-6-methoxy

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:354574-31-5 SDS

354574-31-5Relevant articles and documents

The cooperative FeCl3/DDQ system for the regioselective synthesis of 3-arylindoles from β-monosubstituted 2-alkenylanilines

Jang, Su San,Youn, So Won

, p. 2200 - 2204 (2016/03/01)

A highly regioselective synthesis of 3-arylindoles by using the cooperative FeCl3/DDQ system has been developed. This new protocol represents an attractive route for the synthesis of 3-arylindoles from readily accessible non-indole precursors, β-aryl-substituted 2-styrylanilines, using an inexpensive catalyst and oxidant. Noteworthy is the unique synergetic and synergistic effect of FeCl3 and DDQ on the 1,2-aryl migratory process.

Synthesis of ring-A-substituted tryptophan by a palladium-catalyzed heteroannulation reaction

Jia, Yanxing,Zhu, Jieping

, p. 2469 - 2472 (2007/10/03)

Coupling of substituted o-iodoanilines with methyl (S)-2-N,N-di-tert- butoxycarbonyl-5-oxo-pentanoate, derived from glutamic acid, in DMF in the presence of palladium acetate and DABCO provides substituted tryptophans in good to excellent yields. Georg Thieme Verlag Stuttgart.

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