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17746-05-3

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17746-05-3 Usage

Uses

Undecanoyl chloride has been used in the synthesis of:chrysotrione B, 2-acylcyclopentene-1,3-dione derivative, isolated from the fruiting bodies of the basidiomycete Hygrophorus chrysodon2-methylpentadecan-5-one4-ketotetradecanoic acid

Check Digit Verification of cas no

The CAS Registry Mumber 17746-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,4 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17746-05:
(7*1)+(6*7)+(5*7)+(4*4)+(3*6)+(2*0)+(1*5)=123
123 % 10 = 3
So 17746-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H21ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3

17746-05-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H56380)  n-Undecanoyl chloride, 98%   

  • 17746-05-3

  • 500mg

  • 693.0CNY

  • Detail
  • Alfa Aesar

  • (H56380)  n-Undecanoyl chloride, 98%   

  • 17746-05-3

  • 1g

  • 1764.0CNY

  • Detail
  • Aldrich

  • (249432)  Undecanoylchloride  99%

  • 17746-05-3

  • 249432-500MG

  • 658.71CNY

  • Detail

17746-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Undecanoyl chloride

1.2 Other means of identification

Product number -
Other names n-undecanoyl chloride

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:17746-05-3 SDS

17746-05-3Relevant articles and documents

Optimization of benzoxazinones as natural herbicide models by lipophilicity enhancement

Macias, Francisco A.,Marin, David,Oliveros-Bastidas, Alberto,Molinillo, Jose M. G.

, p. 9357 - 9365 (2006)

Benzoxazinones are plant allelochemicals well-known for their phytotoxic activity and for taking part in the defense strategies of Gramineae, Ranunculaceae, and Scrophulariceae plants. These properties, in addition to the recently optimized methodologies for their large-scale isolation and synthesis, have made some derivatives of natural products, 2,4-dihydroxy-(2H)-1,4- benzoxazin-3-(4H)-one (DIBOA) and its 7-methoxy analogue (DIMBOA), successful templates in the search for natural herbicide models. These new chemicals should be part of integrated methodologies for weed control. In ongoing research about the structure-activity relationships of benzoxazinones and the structural requirements for their phytotoxicity enhancement and after characterization of the optimal structural features, a new generation of chemicals with enhanced lipophilicity was developed. They were tested on selected standard target species and weeds in the search for the optimal aqueous solubility-lipophilicity rate for phytotoxicity. This physical parameter is known to be crucial in modern drug and agrochemical design strategies. The new compounds obtained in this way had interesting phytotoxicity profiles, empowering the phytotoxic effect of the starting benzoxazinone template in some cases. Quantitative structure-activity relationships were obtained by bioactivity-molecular parameters correlations. Because optimal lipophilicity values for phytotoxicity vary with the tested plant, these new derivatives constitute a more selective way to take advantage of benzoxazinone phytotoxic capabilities.

Mild methods to assemble and pattern organic monolayers on hydrogen-terminated Si(111)

Arafat, Samer N.,Dutta, Samrat,Perring, Mathew,Mitchell, Michael,Kenis, Paul J. A.,Bowden, Ned B.

, p. 3198 - 3200 (2005)

Mild methods to assemble well-ordered organic monolayers of olefins on Si(111) using 2,2,6,6-tetramethyl-1-piperidinyloxy and to pattern these monolayers on the micrometer-size scale using soft lithography are reported. The Royal Society of Chemistry 2005.

Characterization of the molecular packing, thermotropic phase behaviour and critical micellar concentration of a homologous series of N-acyltaurines (n = 9–18). PXRD, DSC and fluorescence spectroscopic studies

Arul Prakash, Sukanya,Kamlekar, Ravi Kanth

, (2020/06/22)

N-acyltaurines (NATs) are amides of fatty acids that can be structurally related to endocannabinoids. They show interesting physiological and pharmacological properties. We have synthesized a homologous series of NATs with saturated acyl chains (n = 9–18) and investigated their supramolecular structure and thermotropic phase transitions by powder X-ray diffraction (PXRD) and differential scanning calorimetry (DSC). The d-spacings obtained from PXRD increase linearly with chain length with an increment of ~0.847 ? per additional CH2 moiety suggesting that NATs adopt a tilted bilayer structure with similar packing in crystal lattice. Results obtained from DSC studies indicate that the endothermic transition temperature (Tt) of NATs showed a gradually increasing trend with increasing acyl chain length. The enthalpy (ΔHt) and entropy (ΔSt) of transition show odd-even alternations with odd-chain compounds having higher values than the even-chain compounds. The critical micellar concentration (CMC) of NATs was determined in water at room temperature by fluorescence spectroscopy by monitoring the spectral changes of 8-anilinonaphthalene-1-sulfonic acid (ANS). The CMCs of NATs were found to decrease with increase in acyl chain length. The present results provide a thermodynamic and structural basis for investigating the interaction of NATs with other membrane lipids and proteins, which in turn can shed light in understanding how they function in vivo (in biological membranes).

PYRROLE DERIVATIVES AS ACC INHIBITORS

-

Page/Page column 48; 49, (2019/07/19)

Novel pyrrole derivatives of Formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of Acetyl- CoA carboxylase (ACC).

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