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4378-55-6

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4378-55-6 Usage

General Description

5-(3,4-Dimethoxyphenyl)-5-oxovaleric acid is a chemical compound with the molecular formula C13H16O6. It is a derivative of valeric acid and contains a five-carbon chain with a ketone group and a phenyl ring with two methoxy groups. 5-(3,4-DIMETHOXYPHENYL)-5-OXOVALERIC ACID is commonly used as a building block in organic synthesis and pharmaceutical research. It has potential applications in the development of new drugs and bioactive molecules due to its structural characteristics. Additionally, it may have industrial uses as a precursor in the production of various chemical compounds. Overall, 5-(3,4-Dimethoxyphenyl)-5-oxovaleric acid is an important intermediate compound with diverse potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 4378-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4378-55:
(6*4)+(5*3)+(4*7)+(3*8)+(2*5)+(1*5)=106
106 % 10 = 6
So 4378-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O5/c1-17-11-7-6-9(8-12(11)18-2)10(14)4-3-5-13(15)16/h6-8H,3-5H2,1-2H3,(H,15,16)

4378-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3,4-dimethoxyphenyl)-5-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4378-55-6 SDS

4378-55-6Relevant articles and documents

Design and synthesis of 4,5,6,7‐tetrahydro‐1H‐1,2‐diazepin‐7‐one derivatives as a new series of Phosphodiesterase 4 (PDE4) inhibitors

Guariento, Sara,Karawajczyk, Anna,Bull, James A.,Marchini, Gessica,Bielska, Martyna,Iwanowa, Xenia,Bruno, Olga,Fossa, Paola,Giordanetto, Fabrizio

, p. 24 - 29 (2017)

Phosphodiesterase 4 (PDE4) inhibitors have attractive therapeutic potential in respiratory, inflammatory, metabolic and CNS disorders. The present work details the design, chemical exploration and biological profile of a novel PDE4 inhibitor chemotype. A

Iridium/f-Amphol-catalyzed Efficient Asymmetric Hydrogenation of Benzo-fused Cyclic Ketones

Yin, Congcong,Dong, Xiu-Qin,Zhang, Xumu

supporting information, p. 4319 - 4324 (2018/10/15)

Iridium/f-Amphol-catalyzed asymmetric hydrogenation of various benzo-fused five to seven-membered cyclic ketones was successfully developed, affording a series of chiral benzo-fused cyclic alcohols with excellent results (75%–99% yields, 93%–>99% ee, and TON up to 297 000). The enantioenriched products can be employed as key intermediates or motifs for the synthesis of some important biologically active compounds, such as rasagiline mesylate TVP-1012 used for the treatment of Parkinson's disease, the enantiomer of anticonvulsant drug eslicarbazepine acetate (BIA 2-093). (Figure presented.).

Increasing the open circuit voltage of bulk-heterojunction solar cells by raising the LUMO level of the acceptor

Kooistra, Floris B.,Knol, Joop,Kastenberg, Fredrik,Popescu, Lacramioara M.,Verhees, Wiljan J. H.,Kroon, Jan M.,Hummelen, Jan C.

, p. 551 - 554 (2007/10/03)

We report the synthesis, characterization, and electrochemical properties of ten new fullerene derivatives for usage in organic solar cells. The phenyl ring of PCBM was substituted with electron-donating and electron-withdrawing substituents to study thei

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