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[1,1'-Binaphthalene]-1,1'(2H,2'H)-diol, 3,3',4,4'-tetrahydrois a chemical compound with the chemical formula C22H20O2, also known as 3,3',4,4'-tetrahydro-1,1'-bi-2-naphthol. It is a type of naphthol, composed of two naphthalene rings linked by a carbon-carbon bond and featuring a tetrahydro structure with four hydrogen atoms bonded to a cyclohexene ring.

3073-53-8

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3073-53-8 Usage

Uses

Used in Organic Chemistry:
[1,1'-Binaphthalene]-1,1'(2H,2'H)-diol, 3,3',4,4'-tetrahydrois used as a chiral auxiliary for [asymmetric synthesis] in [organic chemistry] because of its unique structure that aids in the creation of enantiomerically pure compounds.
Used in Pharmaceutical Applications:
[1,1'-Binaphthalene]-1,1'(2H,2'H)-diol, 3,3',4,4'-tetrahydrois used as a [ligand] for [asymmetric catalysis] in the development of pharmaceuticals, playing a crucial role in enhancing the selectivity of reactions to produce desired enantiomers with high purity.
Used in Chemical Research:
[1,1'-Binaphthalene]-1,1'(2H,2'H)-diol, 3,3',4,4'-tetrahydrois also utilized in [chemical research] for studying its potential applications in various fields, including material science and drug discovery, due to its distinctive structural properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 3073-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3073-53:
(6*3)+(5*0)+(4*7)+(3*3)+(2*5)+(1*3)=68
68 % 10 = 8
So 3073-53-8 is a valid CAS Registry Number.

3073-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4-tetrahydro-1-(1,2,3,4-tetrahydro-1-hydroxynaphthalen-1-yl)naphthalen-1-ol

1.2 Other means of identification

Product number -
Other names 3,3',4,4'-tetrahydro[1,1'-binaphthalene]-1,1'(2H,2H')-diol

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:3073-53-8 SDS

3073-53-8Downstream Products

3073-53-8Relevant academic research and scientific papers

Sodium amalgam mediated desulfonylative reduction of α-functionalized β-ketosulfones

Chan, Chieh-Kai,Huang, Yi-Hsuan,Chang, Meng-Yang

, p. 5521 - 5529 (2016/08/04)

Sodium amalgam mediated desulfonylative reduction of β-ketosulfones in MeOH at rt affords alcohols in good yields via radical desulfonylation of β-ketosulfones and sequential Bouveault-Blanc reduction of the resulting ketones.

Light-induced Reactions of 2-(N-Alkyl-N-arylamino)acetophenones and Related Amino-ketones: Formation of 1,3-Diarylazetidin-3-ols

Allworth, Keith L.,EI-Hamamy, Ahmad A.,Hesabi, Massoud M.,Hill, John

, p. 1671 - 1678 (2007/10/02)

On irradiation in ether, 2-(N-methylanilino)acetophenones, Ar1NMe-CH2COAr2 (Ar1,Ar2=Ph,Ph; Ph,p-MeO-C6H4; Ph,p-Ph-C6H4; p-Cl-C6H4,Ph; p-MeO-C6H4,Ph; and p-Me-C6H4,Ph), underwent type II cyclisation to isomeric 1,3-diarylazetidin-3-ols.A minor photoproduct was one of the two expected type II fission products, the corresponding acetophenone Ar2COMe.The second type II fission product, imine Ar1N=CH2, was not detected, but in three cases a 1,3-diarylimidazolidine, probably derived from this imine, was isolated.Similar results were obtained on irradiation of the related amino-ketones, 2-(N-methylanilino)-2'-acetonaphthone and 2-(N-methylanilino)-1-tetralone.Direct fission of the C-2-N bond occured on irradiation of 2-(N-methylanilino)indan-1-one and 2,2-dimethyl-2-(N-methylanilino)acetophenone. 2-(N-Alkylanilino)acetophenones, PhNR-CH2COPh (R=Et, Me2CH, and PHCH2), yielded complex mixtures on irradiation.

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