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65490-09-7

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65490-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65490-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65490-09:
(7*6)+(6*5)+(5*4)+(4*9)+(3*0)+(2*0)+(1*9)=137
137 % 10 = 7
So 65490-09-7 is a valid CAS Registry Number.

65490-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-hydroxy-4,6-bis(methoxymethoxy)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone

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:65490-09-7 SDS

65490-09-7Relevant articles and documents

Neuroregenerative Potential of Prenyl- And Pyranochalcones: A Structure-Activity Study

Aigner, Ludwig,Bieler, Lara,Couillard-Despres, Sebastien,Priglinger, Eleni,Riepl, Herbert M.,Urmann, Corinna

supporting information, p. 2675 - 2682 (2021/10/12)

Loss of neuronal tissue is a hallmark of age-related neurodegenerative diseases. Since adult neurogenesis has been confirmed in the human brain, great interest has arisen in substances stimulating the endogenous neuronal regeneration mechanism based on ad

Synthesis of rottlerone analogues and evaluation of their -glucosidase and DPP-4 dual inhibitory and glucose consumption-promoting activity

Dodd, Robert H.,Lu, Kui,Sun, Hua,Wang, Haibo,Wu, Yan,Yan, Zhihong,Yu, Peng,Zhang, Yinan,Zhao, Xue

, (2021/06/12)

Our previous study found that desmethylxanthohumol (1) inhibited α-glucosidase in vitro. Recently, further investigations revealed that dehydrocyclodesmethylxanthohumol (2) and its dimer analogue rottlerone (3) exhibited more potent α-glucosidase inhibito

An Efficient Regioselective Synthesis of 8-Formylhomoisoflavonoids with Neuroprotective Activity by Enhancing Autophagy

Li, Jie,Yang, Fan,Zeng, Lin-Wei,Zhang, Fang-Min,Zhou, Chang-Xin,Gan, Li-She

, p. 1385 - 1391 (2021/04/12)

6-Formylisoophiopogonone B (7a) and 8-formylophiopogonone B (7b), two natural products isolated fromOphiopogonjaponicus, represent a subgroup of rare 6/8-formyl/methyl-homoisoflavonoid skeletons. Herein we report an efficient method for the synthesis of these formyl/methyl-homoisoflavonoids. The synthesized compounds were evaluated for their neuroprotective effects on the MPP+-induced SH-SY5Y cell injury model and showed marked activity. Exploration of the neuroprotective mechanisms of compound7bled to an increased expression of autophagy marker LC3-II and down-regulation of autophagy substrate p62/SQSTM1. Molecular docking studies showed that7bmay prevent the inhibition of the classic PI3K-AKT-mTOR signaling pathway by interfering with the human HSP90AA1.

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