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29754-58-3

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29754-58-3 Usage

General Description

3-CARBOMETHOXY-4-HYDROXYPHENYLGLYOXAL HYDRATE is a chemical compound that is commonly used in organic synthesis and pharmaceutical research. It is a hydrate of 3-carbomethoxy-4-hydroxyphenylglyoxal, which is a key intermediate in the synthesis of various pharmaceuticals and bioactive compounds. 3-CARBOMETHOXY-4-HYDROXYPHENYLGLYOXAL HYDRATE has been studied for its potential therapeutic applications in the treatment of neurological disorders and cancer. It is also used as a reagent in the synthesis of complex organic molecules. 3-CARBOMETHOXY-4-HYDROXYPHENYLGLYOXAL HYDRATE is a valuable chemical building block that has a wide range of applications in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 29754-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,5 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29754-58:
(7*2)+(6*9)+(5*7)+(4*5)+(3*4)+(2*5)+(1*8)=153
153 % 10 = 3
So 29754-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O5.H2O/c1-15-10(14)7-4-6(9(13)5-11)2-3-8(7)12;/h2-5,12H,1H3;1H2

29754-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 5-(Dihydroxyacetyl)salicylate

1.2 Other means of identification

Product number -
Other names methyl 2-hydroxy-5-oxaldehydoylbenzoate,hydrate

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:29754-58-3 SDS

29754-58-3Relevant articles and documents

A chromatography-free synthesis of racemic salbutamol hemisulfate

Vanoost, Agathe,Petit, Laurent

, (2020/06/30)

Our efforts to achieve an efficient synthesis of racemic salbutamol hemisulfate are described. The selected chemical route starts from commodity chemicals and allows the generation of salbutamol hemisulfate in 5 steps and 44% overall yield without any purification by column chromatography. The reaction sequence has been optimized to provide the title compound using robust procedures. Emphasis on reproducibility and experimental simplicity drove the work described herein.

β2-adrenergic receptor agonists

-

, (2008/06/13)

The present invention is directed to multibinding compounds which are β2 adrenergic receptor agonists and are therefore useful in the treatment and prevention of respiratory diseases such asthma, bronchitis, and the like. They are also useful in the treat

Saligenin analogs of sympathomimetic catecholamines.

Collin,Hartley,Jack,Lunts,Press,Ritchie,Toon

, p. 674 - 680 (2007/10/04)

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