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3-methoxy-4-(methoxymethoxy)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98960-08-8

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98960-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98960-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,6 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98960-08:
(7*9)+(6*8)+(5*9)+(4*6)+(3*0)+(2*0)+(1*8)=188
188 % 10 = 8
So 98960-08-8 is a valid CAS Registry Number.

98960-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-4-(methoxymethoxy)aniline

1.2 Other means of identification

Product number -
Other names ANILINE,3-METHOXY-4-(METHOXYMETHOXY)

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:98960-08-8 SDS

98960-08-8Downstream Products

98960-08-8Relevant academic research and scientific papers

Discovery of highly potent human glutaminyl cyclase (QC) inhibitors as anti-Alzheimer's agents by the combination of pharmacophore-based and structure-based design

Ann, Jihyae,Ha, Hee-Jin,Ha, Jung-Hye,Hoang, Van-Hai,Jang, Tae-ho,Kim, Hee,Kim, Young-Ho,Lee, Jeewoo,Lee, Jiyoun,Ngo, Van T. H.,Song, Jae Young,Van Manh, Nguyen

, (2021/09/20)

The inhibition of glutaminyl cyclase (QC) may provide a promising strategy for the treatment of early Alzheimer's disease (AD) by reducing the amount of the toxic pyroform of β-amyloid (AβΝ3pE) in the brains of AD patients. In this work, we ide

Design, synthesis, and biological evaluation of quinazoline derivatives as dual HDAC1 and HDAC6 inhibitors for the treatment of cancer

Chen, Jinying,Sang, Zitai,Jiang, Youjun,Yang, Chao,He, Linhong

, p. 232 - 241 (2018/11/02)

Fifty-eight quinazoline-based compounds were designed and synthesized based on the structural optimizations from the lead compound 23bb in an attempt to search for more potent dual HDAC1 and HDAC6 inhibitors. Among them, 32c (HDAC1, IC50?=?31.1

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