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58045-41-3

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58045-41-3 Usage

Chemical Properties

Off-White Solid

Uses

Cinnamic Acid derivative

Synthesis Reference(s)

Synthesis, p. 747, 1984 DOI: 10.1055/s-1984-30956

Check Digit Verification of cas no

The CAS Registry Mumber 58045-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58045-41:
(7*5)+(6*8)+(5*0)+(4*4)+(3*5)+(2*4)+(1*1)=123
123 % 10 = 3
So 58045-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O3/c1-14-11(13)7-6-9-2-4-10(8-12)5-3-9/h2-8H,1H3/b7-6+

58045-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-formylcinnamate

1.2 Other means of identification

Product number -
Other names (E)-4-Formylcinnamic Acid Methyl Ester

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:58045-41-3 SDS

58045-41-3Relevant articles and documents

Palladium(II) complexes of (t-butyl salicylidene) diphenyl disulfide diamine: synthesis, structure, spectral characterization and catalytic properties

Bhowon, Minu G.,Jhaumeer Laulloo, Sabina,Hosten, Eric C.,Elaheebacus, Sumayya,Dowlut, Mounisha R.

, p. 537 - 545 (2021)

The hexadentate N2S2O2 donor ligand N,N’-bis(3,5-tert-butylsalicylidene) diphenyl disulfide-2,2’-diamine was synthesised by the condensation of 2-aminophenyl disulfide and 3,5-di-tert-butyl-2-hydroxybenzaldehyde and its mo

Removal of soluble palladium complexes from reaction mixtures by fixed-bed adsorption

Girgis, Michael J.,Kuczynski, Laura E.,Berberena, Sonia M.,Boyd, Caitlin A.,Kubinski, Pamela L.,Scherhob, Megerle L.,Drinkwater, Donald E.,Shen, Xiaoxuan,Babiak, Stanislaw,Lefebvre, Brian G.

, p. 1209 - 1217 (2008)

The increasing use of metal-containing catalysts in producing pharmaceutical intermediates and active pharmaceutical ingredients, in conjunction with requirements of low metal content in a drug substance, has motivated the development of efficient separations processes for metals removal. In this paper, fixed-bed adsorption, an attractive alternative to batch adsorption, was investigated using a reaction mixture from a Heck coupling. Adsorption isotherm determinations using three candidate adsorbents revealed that QuadraPure TU had the greatest affinity and identified the optimal adsorption temperature. The bed residence time was key in obtaining good adsorption efficiency in subsequent fixed-bed experiments. Methods for palladium detection by HPLC were developed to monitor adsorption column performance in quasi real-time. A preliminary design methodology was developed in which actual breakthrough time is estimated from the experimentally determined tradeoff between bed efficiency and residence time. Even at the realized 55% bed efficiency, fixed-bed adsorption requires less than one-fourth the adsorbent needed for a single-stage batch adsorption process.

Curcumin histone deacetylase inhibitor and preparation method and medical application thereof

-

Paragraph 0038-0041, (2021/07/24)

The invention relates to the fields of medicinal chemistry and biology, in particular to a curcumin histone deacetylase inhibitor. The invention also discloses a preparation method of the inhibitor and an application of the inhibitor in exerting anti-tumor activity by inhibiting histone deacetylase.

HISTONE DEACETYLASE 6 INHIBITORS AND METHOD FOR TREATING NEUROPATHIC PAIN

-

Paragraph 0068; 0082-0083, (2021/01/29)

Disclosed herein are hydroxamic acid compounds. Also disclosed is a method of using the hydroxamic acid compounds for treating a condition associated with histone deacetylase 6.

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