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all-trans-retinal dimer is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193532-21-7

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193532-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193532-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,5,3 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 193532-21:
(8*1)+(7*9)+(6*3)+(5*5)+(4*3)+(3*2)+(2*2)+(1*1)=137
137 % 10 = 7
So 193532-21-7 is a valid CAS Registry Number.

193532-21-7Downstream Products

193532-21-7Relevant academic research and scientific papers

Aberrant buildup of all-Trans-retinal dimer, a nonpyridinium bisretinoid lipofuscin fluorophore, contributes to the degeneration of the retinal pigment epithelium

Zhao, Junli,Liao, Yi,Chen, Jingmeng,Dong, Xinran,Gao, Zhan,Zhang, Houjian,Wu, Xiaodan,Liu, Zuguo,Wu, Yalin

, p. 1063 - 1075 (2017)

PURPOSE. Nondegradable fluorophores that accumulate as deleterious lipofuscin of RPE are involved in pathological mechanisms leading to the degeneration of RPE in AMD. A2E, a major component of RPE lipofuscin, could cause damage to RPE cells. Nevertheless

Condensation of all-E-retinal

Verdegem, Peter J. E.,Monnee, Menno C. F.,Mulder, Patrick P. J.,Lugtenburg, Johan

, p. 5355 - 5358 (1997)

A novel base induced self condensation product of all-E-retinal is presented. The scope of the reaction is investigated with three analogous α,β-unsaturated aldehydes.

Substituted Cyclohexadienals - Syntheses and Applications

-

Page/Page column 18-19, (2010/11/28)

The present invention is generally directed to the use of L-proline and certain derivatives thereof to catalyze the asymmetric self-condensation of α,β-unsaturated aldehydes to form homodimer and heterodimer cyclohexadienals. Reaction conditions are mild

The proline and β-lactoglobulin mediated asymmetric self-condensation of β-ionylideneacetaldehyde, retinal and related compounds

Asato,Watanabe,Li,Liu

, p. 3105 - 3108 (2007/10/02)

Proline was found to effectively mediate the asymmetric reaction of β-ionylideneacetaldehyde 1A, retinal and related α,β-unsaturated aldehydes to form their corresponding self-condensation products in reasonable enantiomeric excess (up to 65% ee). This sa

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