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106018-39-7

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106018-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106018-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,1 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 106018-39:
(8*1)+(7*0)+(6*6)+(5*0)+(4*1)+(3*8)+(2*3)+(1*9)=87
87 % 10 = 7
So 106018-39-7 is a valid CAS Registry Number.

106018-39-7SDS

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-hydroxy-benzoic acid-(2-morpholino-ethylamide)

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-benzoesaeure-(2-morpholino-aethylamid)

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:106018-39-7 SDS

106018-39-7Downstream Products

106018-39-7Relevant articles and documents

Design, synthesis, and evaluation of simple phenol amides as ERRγ agonists

Lin, Hua,Doebelin, Christelle,Patouret, Rémi,Garcia-Ordonez, Ruben D.,Ra Chang, Mi,Dharmarajan, Venkatasubramanian,Bayona, Claudia Ruiz,Cameron, Michael D.,Griffin, Patrick R.,Kamenecka, Theodore M.

, p. 1313 - 1319 (2018/03/21)

Herein we report the design and synthesis of a series of simple phenol amide ERRγ agonists based on a hydrazone lead molecule. Our structure activity relationship studies in this series revealed the phenol portion of the molecule to be required for activity. Attempts to replace the hydrazone with more suitable chemotypes led to a simple amide as a viable alternative. Differential hydrogen-deuterium exchange experiments were used to help understand the structural basis for binding to ERRγ and aid in the development of more potent ligands.

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