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Carbamic acid, [(2-iodophenyl)methyl]-, methyl ester is a chemical compound with the molecular formula C9H9INO2. It is a versatile and reactive intermediate used in the synthesis of pharmaceuticals and agrochemicals, as well as a potential precursor for various organic compounds.

90679-69-9

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90679-69-9 Usage

Uses

Used in Pharmaceutical Industry:
Carbamic acid, [(2-iodophenyl)methyl]-, methyl ester is used as an intermediate in the synthesis of pharmaceuticals for its reactivity and versatility, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Carbamic acid, [(2-iodophenyl)methyl]-, methyl ester is also utilized as an intermediate in the production of agrochemicals, playing a role in the development of pesticides, herbicides, and other agricultural products to improve crop yield and protect plants from pests.
Safety and Environmental Considerations:

Check Digit Verification of cas no

The CAS Registry Mumber 90679-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,7 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90679-69:
(7*9)+(6*0)+(5*6)+(4*7)+(3*9)+(2*6)+(1*9)=169
169 % 10 = 9
So 90679-69-9 is a valid CAS Registry Number.

90679-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-[(2-iodophenyl)methyl]carbamate

1.2 Other means of identification

Product number -
Other names methyl (2-iodobenzyl)carbamate

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:90679-69-9 SDS

90679-69-9Relevant academic research and scientific papers

Intramolecular trapping of allenylzincs by carbonyl groups

Jammi, Suribabu,Maury, Julien,Suppo, Jean-Simon,Bertrand, Michele P.,Feray, Laurence

, p. 12566 - 12576 (2014/01/17)

Allenylzinc formed via oxygen-promoted zinc/iodine exchange between propargyl iodides and diethylzinc can be trapped by intramolecular reaction with various electrophiles such as aldehydes, ketones, esters, carbamates, and imides. Potentially useful build

Radical dearomatization of benzene leading to phenanthridine and phenanthridinone derivatives related to (±)-pancratistatin

Crich, David,Krishnamurthy, Venkataramanan

, p. 6830 - 6840 (2007/10/03)

The synthesis of the phenanthridinone nucleus common to the Amaryllidaceae series of natural products is achieved by a sequence involving tributylstannane-mediated, benzeneselenol-catalyzed addition of ortho-nitrogen functionalized aryl radicals to benzen

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