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7064-38-2

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7064-38-2 Usage

General Description

4-Iodo-5-methyl-isoxazole, also known as IMI, is a chemical compound with the molecular formula C4H4INO. It is a ring-substituted isoxazole derivative with a methyl group and an iodine atom attached to the five-membered ring. IMI is used as a building block in organic synthesis and pharmaceutical research. It can also act as a ligand in coordination chemistry and catalysis. IMI is primarily produced through a series of chemical reactions involving the selective functionalization of the isoxazole ring, and it is a versatile intermediate for the synthesis of various biologically active compounds and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 7064-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7064-38:
(6*7)+(5*0)+(4*6)+(3*4)+(2*3)+(1*8)=92
92 % 10 = 2
So 7064-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H4INO/c1-3-4(5)2-6-7-3/h2H,1H3

7064-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-5-methyl-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 5-methyl-4-iodoisoxazole

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:7064-38-2 SDS

7064-38-2Upstream product

7064-38-2Relevant articles and documents

Enantioselective organo-SOMO cascade cycloadditions: A rapid approach to molecular complexity from simple aldehydes and olefins

Jui, Nathan T.,Lee, Esther C. Y.,MacMillan, David W. C.

supporting information; experimental part, p. 10015 - 10017 (2010/10/03)

A highly selective, radical-mediated (4 + 2) coupling reaction of aldehydes and conjugated olefins has been achieved through asymmetric SOMO-catalysis. A radical-polar crossover mechanism is proposed wherein olefin addition to a transient enamine radical cation and oxidation of the resulting radical furnishes a cation which is vulnerable to nucleophilic addition. A range of aromatic aldehydes are shown to couple with styrenes and dienes to provide cyclic products with high chemical efficiency, regioselectivity, and stereoselectivity.

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