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126085-92-5

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126085-92-5 Usage

General Description

5-Iodo-3-methyl-isoxazole is a chemical compound with the molecular formula C6H5INO. It is an isoxazole derivative, which is a five-membered aromatic ring with an oxygen and a nitrogen heteroatom. 5-Iodo-3-methyl-isoxazole is often used as a building block in organic synthesis, and it has been studied for its potential pharmaceutical applications. 5-Iodo-3-methyl-isoxazole has also been investigated for its pesticidal properties, and it is known to have antimicrobial and antifungal activity. Furthermore, it is considered to be a potential precursor in the synthesis of various pharmaceuticals and agrochemicals. Overall, 5-Iodo-3-methyl-isoxazole has a wide range of potential applications in the fields of pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 126085-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,0,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126085-92:
(8*1)+(7*2)+(6*6)+(5*0)+(4*8)+(3*5)+(2*9)+(1*2)=125
125 % 10 = 5
So 126085-92-5 is a valid CAS Registry Number.

126085-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodo-3-methylisoxazole

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:126085-92-5 SDS

126085-92-5Downstream Products

126085-92-5Relevant articles and documents

The synthesis of epiboxidine and related analogues as potential pharmacological agents

Kulu, Irem,Ocal, Nuket

scheme or table, p. 2054 - 2060 (2012/01/04)

Methyl epiboxidine-N-carboxylate (8) was synthesized from 7 under reductive Heck conditions (Scheme 2). The C-C coupling of the new epiboxidine analog 9 with aryl and heteroaryl halides gave by hydroarylation C-aryl, N-(3-methylisoxazol-5-yl)-substituted

SYNTHESIS AND REACTIONS OF 5-(TRIBUTYLSTANNYL)ISOXAZOLES

Kondo, Yoshinori,Uchiyama, Daishi,Sakamoto, Takao,Yamanaka, Hiroshi

, p. 4249 - 4250 (2007/10/02)

3-Substituted 5-(tributylstannyl)isoxazoles were synthesized in good yields by the 1,3-dipolar cycloaddition reaction of ethynyltributylstannane with nitrile oxides generated in situ. 3-Methyl-5-(tributylstannyl)isoxazole was easily converted to the corre

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