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60345-97-3

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60345-97-3 Usage

General Description

3-(2-Hydroxyethoxy)benzaldehyde is a chemical compound with the molecular formula C9H10O3. It is mainly used in the production of pharmaceuticals, dyes, and perfumes. The chemical is characterized by its benzaldehyde core with a hydroxyethoxy group attached to the benzene ring at the 3-position. 3-(2-HYDROXYETHOXY)BENZALDEHYDE is utilized as a precursor in organic synthesis and as a reagent in various chemical reactions. Its aromatic properties make it valuable in the fragrance industry, while its reactivity and functional groups make it useful in pharmaceutical and dye synthesis. Additionally, it is known for its potential antimicrobial and antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 60345-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,4 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60345-97:
(7*6)+(6*0)+(5*3)+(4*4)+(3*5)+(2*9)+(1*7)=113
113 % 10 = 3
So 60345-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O3/c10-4-5-12-9-3-1-2-8(6-9)7-11/h1-3,6-7,10H,4-5H2

60345-97-3SDS

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-(2-Hydroxyethoxy)benzaldehyde

1.2 Other means of identification

Product number -
Other names 3-(2-HYDROXYETHOXY)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:60345-97-3 SDS

60345-97-3Relevant articles and documents

A molybdenum based metallomicellar catalyst for controlled and chemoselective oxidation of activated alcohols in aqueous medium

Thiruvengetam, Prabaharan,Chakravarthy, Rajan Deepan,Chand, Dillip Kumar

, p. 123 - 133 (2019/07/19)

A surfactant based oxodiperoxo molybdenum complex, which could activate molecular oxygen, has been employed as a catalyst for controlled oxidation of benzylic alcohols to corresponding carbonyls. The oxidation reactions were carried out under aqueous environment, however, in the absence of any extraneous base or co-catalyst. Sensitive/oxidizable functional groups like cyano, sulfide, hydroxyl, aryl-hydroxyl, alkene (internal/terminal), alkyne (internal/terminal), and acetal were tolerated during the transformations. Such selectivity is attributed to the mild nature of the catalyst. The methodology could also be scaled-up for multi-gram synthesis and the protocol is likely to find practical use since it requires an inexpensive recyclable-catalyst and easily available oxidant (under green conditions). A plausible mechanism is proposed with the help of preliminary computational study.

COMPOSITIONS, METHODS, AND SYSTEMS FOR THE SYNTHESIS AND USE OF IMAGING AGENTS

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Paragraph 1534, (2015/07/22)

The present invention provides compounds with imaging moieties for imaging a subject. The present invention also relates to systems, compositions, and methods for the synthesis and use of imaging agents, or precursors thereof. An imaging agent precursor may be converted to an imaging agent using the methods described herein. In some cases, a composition or plurality of imaging agents is enriched in 18 F. In some cases, an imaging agent may be used to image an area of interest in a subject, including, but not limited to, the heart, cardiovascular system, cardiac vessels, brain, and other organs.

Photoactivatable fluorescein derivatives caged with a (3-hydroxy-2- naphthalenyl)methyl group

Nekongo, Emmanuel E.,Popik, Vladimir V.

, p. 7665 - 7671 (2014/09/17)

The (3-hydroxy-2-naphthalenyl)methyl (NQMP) group represents an efficient photocage for fluorescein-based dyes. Thus, irradiation of the 6-NQMP ether of 2'-hydroxymethylfluorescein with low-intensity UVA light results in a 4-fold increase in emission inte

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