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14621-59-1

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14621-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14621-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,2 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14621-59:
(7*1)+(6*4)+(5*6)+(4*2)+(3*1)+(2*5)+(1*9)=91
91 % 10 = 1
So 14621-59-1 is a valid CAS Registry Number.

14621-59-1SDS

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 2-(naphthalen-1-yloxy)-1-phenylethanone

1.2 Other means of identification

Product number -
Other names 2-[1]Naphthyloxy-1-phenyl-aethanon

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:14621-59-1 SDS

14621-59-1Relevant articles and documents

Synthesis of coumarin derivatives as inhibitors of platelet aggregation

Chen, Yeh-Long,Wang, Tai-Chi,Lee, Kuan-Han,Tzeng, Cherng-Chyi,Chang, Ya-Ling,Teng, Che-Ming

, p. 651 - 657 (1996)

In a search for the inhibitors of platelet aggregation, certain coumarin derivatives were synthesized and evaluated for antiplatelet activity against thrombin(Thr)-, arachidonic acid(AA)-, collagen(Col)-, and platelet-activating-factor(PAF)-induced aggreg

Synthesis of benzofurans from the cyclodehydration of α-phenoxy ketones mediated by Eaton’s reagent

Ma, Lin,Ma, Zhanwei,Zhang, Min,Zhou, Min

, p. 426 - 436 (2020/03/23)

Cyclodehydration of α-phenoxy ketones promoted by Eaton’s reagent (phosphorus pentoxide–methanesulfonic acid) is used to prepare 3-substituted or 2,3-disubstituted benzofurans with moderate to excellent yields under mild conditions. The method provides a facile access to benzofurans from readily available starting materials such as phenols and α-bromo ketones. The reaction is highly efficient, which is attributed to the good reactivity and fluidity of Eaton’s reagent. The reaction can be applied to prepare naphthofurans, furanocoumarins, benzothiophenes, and benzopyrans.

Discovery of oxime-bearing naphthalene derivatives as a novel structural type of Nrf2 activators

Chang, Ken-Ming,Liang, Fong-Pin,Chen, I-Li,Yang, Shyh-Chyun,Juang, Shin-Hun,Wang, Tai-Chi,Chen, Yeh-Long,Tzeng, Cherng-Chyi

, p. 3852 - 3859 (2015/08/03)

Abstract Recent studies have demonstrated that oxidative stress insult is one of major causes of tumor formation. Therefore, identify the effective anti-oxidative agents as a preventive approach to stop cancer progression has widely explored. Although, ma

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