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24083-19-0

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24083-19-0 Usage

Chemical Properties

slightly yellow to beige low melting solid

Check Digit Verification of cas no

The CAS Registry Mumber 24083-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,8 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24083-19:
(7*2)+(6*4)+(5*0)+(4*8)+(3*3)+(2*1)+(1*9)=90
90 % 10 = 0
So 24083-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H30O2/c1-2-3-4-5-6-7-8-9-10-11-16-21-19-14-12-18(17-20)13-15-19/h12-15,17H,2-11,16H2,1H3

24083-19-0 Well-known Company Product Price

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  • Alfa Aesar

  • (L08889)  4-n-Dodecyloxybenzaldehyde, 98%   

  • 24083-19-0

  • 1g

  • 300.0CNY

  • Detail
  • Alfa Aesar

  • (L08889)  4-n-Dodecyloxybenzaldehyde, 98%   

  • 24083-19-0

  • 5g

  • 1107.0CNY

  • Detail

24083-19-0SDS

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 4-dodecoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names p-Dodecyloxybenzaldehyde

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:24083-19-0 SDS

24083-19-0Relevant articles and documents

Giant porphyrin disks: Control of their self-assembly at liquid-solid interfaces through metal-ligand interactions

Lensen, Marga C.,Elemans, Johannes A. A. W.,Van Dingenen, Sandra J. T.,Gerritsen, Jan W.,Speller, Sylvia,Rowan, Alan E.,Nolte, Roeland J. M.

, p. 7948 - 7956 (2007)

The synthesis and self-assembly behaviour of porphyrin dodecamers 1H 2 and Zn-1, which consist of twelve porphyrins that are covalently attached to a central aromatic core, is described. According to STM, 1D and 2D NMR studies, and molecular mo

Mesogenic complementary absorbing dyads based on porphyrin and perylene units

Kong, Xiangfei,Gong, Hongkang,Dai, Shengping,Yao, Wei,Mu, Linping,Zhang, Shufen,Wang, Guixia

, p. 221 - 232 (2018)

Five novel dyads, consisting of a tetraphenylporphyrine unit connected to a perylene monoimide diester unit via a flexible bridge-CONH-(CH2)n-(n = 4, 6, 8, 10 and 12), have been synthesized. Their structures were characterized by 13C and 1H nuclear magnet

Near-infrared fluorescent amphiphilic Aza-BODIPY dye: Synthesis, solvatochromic properties, and selective detection of Cu2+

Chen, Yuanfang,Chen, Zhijian,Pan, Hongfei,Ren, Xiang-Kui,Wang, Houchen,Zhang, Yongjie,Zuo, Jiahe

, (2020)

A new amphiphilic near-infrared aza-BODIPY dye bearing both hydrophobic alkyl and hydrophilic oligo-ethylene glycol chains was synthesized by facile click reaction. By introducing the electron-donating N,N-disubstituted amino groups into the molecular str

Concentration and acid-base controllable fluorescence of a metallosupramolecular polymer

He, Lipeng,Liang, Jianjun,Cong, Yong,Chen, Xin,Bu, Weifeng

, p. 10841 - 10844 (2014)

A metallosupramolecular polymer (MP-Zn) bearing dibenzo-24-crown-8 (DB24C8) arms is constructed by coordinating Zn2+ with a conjugated bis-terpyridine ligand, which indicates concentration-dependent emissions from cyan to white to yellow. Succe

Metal-free C-H functionalization of pyrrolidine to pyrrolinium-based room temperature ionic liquid crystals

Mandal, Sumana,Gupta, Ravindra Kumar,Pathak, Suraj Kumar,Rao, D. S. Shankar,Prasad, S. Krishna,Ammathnadu Sudhakar, Achalkumar,Jana, Chandan K.

supporting information, p. 8064 - 8071 (2021/05/21)

The development of ionic liquid crystals (ILCs) using pyrrolidinium cation has received considerable interest due to their higher electrochemical stability. However, high charge density associated with low charge distribution in the fully saturated pyrrol

Synthesis, mesomorphism, photophysics and device performance of liquid-crystalline pincer complexes of gold(iii)

Parker, Rachel R.,Liu, Denghui,Yu, Xiankang,Whitwood, Adrian C.,Zhu, Weiguo,Williams,Wang, Yafei,Lynam, Jason M.,Bruce, Duncan W.

supporting information, p. 1287 - 1302 (2021/02/12)

Emissive gold(iii) complexes of pincer 2,6-diphenylpyridines also bearing a phenylacetylide ligand have been modified at both the pincer and phenylacetylide to confer liquid crystalline properties, with most complexes showing a columnar hexagonal phase in

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