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4-Isoxazolecarboxylicacid,5-amino-3-methyl-,methylester(8CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23286-53-5

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23286-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23286-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,8 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23286-53:
(7*2)+(6*3)+(5*2)+(4*8)+(3*6)+(2*5)+(1*3)=105
105 % 10 = 5
So 23286-53-5 is a valid CAS Registry Number.

23286-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-amino-3-methyl-1,2-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-ISOXAZOLECARBOXYLIC ACID,5-AMINO-3-METHYL-,METHYL ESTER

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:23286-53-5 SDS

23286-53-5Downstream Products

23286-53-5Relevant academic research and scientific papers

Synthesis of novel 2-(1-adamantanylcarboxamido)thiophene derivatives. Selective cannabinoid type 2 (CB2) receptor agonists as potential agents for the treatment of skin inflammatory disease

Mugnaini, Claudia,Rabbito, Alessandro,Brizzi, Antonella,Palombi, Nastasja,Petrosino, Stefania,Verde, Roberta,Di Marzo, Vincenzo,Ligresti, Alessia,Corelli, Federico

, p. 239 - 251 (2019)

A set of CB2R ligands, based on the thiophene scaffold, was synthesized and evaluated in in vitro assays. Compounds 8c-i, k, l, bearing the 3-carboxylate and 2-(adamantan-1-yl)carboxamido groups together with apolar alkyl/aryl substituents at 5-position or at 4- and 5-positions of the thiophene ring possess high CB2R affinity at low nanomolar concentration, good receptor selectivity, and agonistic functional activity. The full agonist 8g, showing the best balance between receptor affinity and selectivity, was tested in vitro in an experimental model of allergic contact dermatitis and proved to be able to block the release of MCP-2 in HaCaT cells at 10 μM concentration.

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