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Undecan-10-en-1-ylpropanedioic acid is a complex organic compound with the chemical formula C16H28O4. It is a derivative of propanoic acid, featuring an undec-10-en-1-yl group attached to the propanoic acid backbone. This molecule consists of a 10-carbon unsaturated alkyl chain with a double bond, which is connected to the propanoic acid through a carbon-carbon bond. The compound is characterized by its long hydrocarbon chain and carboxylic acid functional groups, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, fragrances, and chemical research.

4475-28-9

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4475-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4475-28-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,7 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4475-28:
(6*4)+(5*4)+(4*7)+(3*5)+(2*2)+(1*8)=99
99 % 10 = 9
So 4475-28-9 is a valid CAS Registry Number.

4475-28-9SDS

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 2-undec-10-enylpropanedioic acid

1.2 Other means of identification

Product number -
Other names Undec-10-enyl-malonsaeure

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:4475-28-9 SDS

4475-28-9Relevant academic research and scientific papers

Total Synthesis of Laucysteinamide A, a Monomeric Congener of Somocystinamide A

Taylor, Kimberly S.,Zhang, Chen,Glukhov, Evgenia,Gerwick, William H.,Suyama, Takashi L.

supporting information, p. 865 - 870 (2021/04/02)

Laucysteinamide A (4) is a marine natural product isolated from the cyanobacterium Caldora penicillata and contains structural motifs found in promising cancer drug leads. The first total synthesis of 4 and its analogues was achieved, which also enabled a concise formal synthesis of somocystinamide A (3), a dimeric congener of 4 that previously showed extremely potent antiproliferative activities. This work provides further insights on structure-activity relationships in this class of natural products.

AVOIDANCE OF NON-SPECIFIC BINDING ON AN ACOUSTIC WAVE BIOSENSOR USING LINKER AND DILUENT MOLECULES FOR DEVICE SURFACE MODIFICATION

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Page/Page column 5, (2012/01/03)

An acoustic wave biosensor comprising a surface of a mixed self-assembling monolayer for receiving a probe-biomolecule is described herein. The biosensor surface may comprise a piezoelectric quartz crystal,—for detection purposes with the electromagnetic piezoelectric acoustic sensor (EMPAS)—upon which a mixed self-assembling monolayer is formed, which includes at least one linker, such as 2,2,2-trifluoroethyl-13-trichlorosilyl-tridecanoate (TTTA); its oligoethylene glycol (OEG) analog OEGylated TTTA (OEG-TTTA); S-(2-(2-(2-(3-trichlorosilyl-propyloxy)-ethoxy)-ethoxy)-ethyl)-benzenethiosulfonate (OEG-TU BTS). Linker/diluent systems for attaching a functionalizing entity to the surface of a biosensor are described, as well as methods for preparing a biosensor surface with an oligoethylene glycol linker.

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