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Isoxazole, 5-[2-(2,4-dichlorophenyl)-2-(3,5-dimethyl-4-isoxazolyl)ethyl]-3-methyl-4- nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78636-36-9

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78636-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78636-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,3 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78636-36:
(7*7)+(6*8)+(5*6)+(4*3)+(3*6)+(2*3)+(1*6)=169
169 % 10 = 9
So 78636-36-9 is a valid CAS Registry Number.

78636-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-(3,5-dimethylisoxazol-5-yl)-2-(2,4-dichlorophenyl)ethyl]-3-methyl-4-nitroisoxazole

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:78636-36-9 SDS

78636-36-9Downstream Products

78636-36-9Relevant academic research and scientific papers

Multicomponent synthesis of 3-heteroarylpropionic acids

Adamo, Mauro F. A.,Duffy, Eleanor F.

, p. 5157 - 5159 (2007/10/03)

(Chemical Equation Presented) A four component one-pot procedure (4-MC) was developed to assemble 3-heteroarylpropionic acids from commercially available materials. This new methodology affords the title compounds in high yields and without the use of chr

Ethylene-diheterocycles: Part I - Synthesis of 5--3-methyl-4-nitroisoxazoles

Rao, C. Janakirama,Reddy, K. Malla,Murthy, A. Krishna

, p. 997 - 998 (2007/10/02)

Michael addition of acetylacetone to 3-methyl-4-nitro-5-styrylisoxazoles (I) in triethylamine leads to 3--2,4-pentanediones (II).The pentanediones (II) undergo cyclisation with hydroxylamine to give 5-ω

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