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(2-acetyl-4,5-dimethoxy-phenoxy)-acetic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

857554-36-0

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857554-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857554-36-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,5,5 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 857554-36:
(8*8)+(7*5)+(6*7)+(5*5)+(4*5)+(3*4)+(2*3)+(1*6)=210
210 % 10 = 0
So 857554-36-0 is a valid CAS Registry Number.

857554-36-0SDS

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 (2-acetyl-4,5-dimethoxy-phenoxy)-acetic acid ethyl ester

1.2 Other means of identification

Product number -
Other names (2-Acetyl-4,5-dimethoxy-phenoxy)-essigsaeure-aethylester

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:857554-36-0 SDS

857554-36-0Relevant academic research and scientific papers

Synthesis and agonistic activity at the GPR35 of 5,6-dihydroxyindole-2- carboxylic acid analogues

Deng, Huayun,Fang, Ye

, p. 550 - 554 (2012)

5,6-Dihydroxyindole-2-carboxylic acid (DHICA), an intermediate of melanin synthesis and an eumelanin building block, was recently discovered to be a GPR35 agonist with moderate potency. Here, we report the synthesis and pharmacological characterization of a series of DHICA analogues against GPR35 using both label-free dynamic mass redistribution and Tango β-arrestin translocation assays. This led to identification of novel GPR35 agonists with improved potency and/or having biased agonism.

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