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6515-21-5

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6515-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6515-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6515-21:
(6*6)+(5*5)+(4*1)+(3*5)+(2*2)+(1*1)=85
85 % 10 = 5
So 6515-21-5 is a valid CAS Registry Number.

6515-21-5SDS

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 4-(methoxymethoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(methoxymethyloxy)benzaldehyde

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:6515-21-5 SDS

6515-21-5Relevant articles and documents

A selective fluorescent sensor for Pb(II) in water

Wu, Fang-Ying,Bae, Se Won,Hong, Jong-In

, p. 8851 - 8854 (2006)

A new fluorescent sensor (1) containing bis(2-pyridylmethyl)amine group as a binding moiety for Pb2+ was developed. Compound 1 shows selective response to Pb2+ over other metal ions in pH 7.0 HEPES buffer solution. The fluorescence i

NaI-mediated oxidative amidation of benzyl alcohols/aromatic aldehydes to benzamides via electrochemical reaction

Rerkrachaneekorn, Tanawat,Tankam, Theeranon,Sukwattanasinitt, Mongkol,Wacharasindhu, Sumrit

supporting information, (2021/04/15)

In this research, we have developed a mild electrochemical process for oxidative amidation of benzyl alcohols/aromatic aldehydes with cyclic amines into the corresponding benzamides. This electroorganic synthetic method proceeds using NaI as a redox mediator under ambient temperature in undivided cell, providing more than 25 examples of amide products in moderate to good yields. The benefits of this reaction include one-pot synthesis, open air condition, proceed in aqueous media and no requirement of external conducting salt, base and oxidant.

Oxoammonium-Mediated Allylsilane–Ether Coupling Reaction

Carlet, Federica,Bertarini, Greta,Broggini, Gianluigi,Pradal, Alexandre,Poli, Giovanni

supporting information, p. 2162 - 2168 (2021/04/02)

A new C(sp3)?H functionalization reaction consisting of the oxidative α-allylation of allyl- and benzyl- methyl ethers has been developed. The C?C coupling could be carried out under mild conditions thanks to the use of cheap and green oxoammonium salts. The scope of the reaction was studied over 27 examples, considering the nature of the substituents on the two coupling partners.

Microbial Transformation of Broussochalcones A and B by Aspergillus niger

Xiao, Yina,Han, Fubo,Kim, Myeong Ji,Lee, Kwang Youl,Lee, Ik-Soo

supporting information, p. 601 - 607 (2021/02/16)

Broussochalcones A (BCA, 1) and B (BCB, 2) are major bioactive constituents isolated from Broussonetia papyrifera, a polyphenol-rich plant belonging to the family Moraceae. Due to their low yields from natural sources, BCA (1) and BCB (2) were prepared sy

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