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825-51-4

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825-51-4 Usage

Chemical Properties

white to light yellow weak paste

Synthesis Reference(s)

Tetrahedron Letters, 22, p. 941, 1981 DOI: 10.1016/0040-4039(81)89014-4

Check Digit Verification of cas no

The CAS Registry Mumber 825-51-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 825-51:
(5*8)+(4*2)+(3*5)+(2*5)+(1*1)=74
74 % 10 = 4
So 825-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h8-11H,1-7H2/t8-,9+,10-/m0/s1

825-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name DECAHYDRO-2-NAPHTHOL

1.2 Other means of identification

Product number -
Other names 2-Hydroxydecalin

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:825-51-4 SDS

825-51-4Relevant articles and documents

Enhancing Chemo- And Stereoselectivity in C-H Bond Oxygenation with H2O2by Nonheme High-Spin Iron Catalysts- And Role of Lewis Acid and Multimetal Centers

Das, Abhishek,Jana, Rahul Dev,Paine, Tapan Kanti

, p. 5969 - 5979 (2021/05/04)

Spin states of iron often direct the selectivity in oxidation catalysis by iron complexes using hydrogen peroxide (H2O2) on an oxidant. While low-spin iron(III) hydroperoxides display stereoselective C-H bond hydroxylation, the reactions are nonstereoselective with high-spin iron(II) catalysts. The catalytic studies with a series of high-spin iron(II) complexes of N4 ligands with H2O2 and Sc3+ reported here reveal that the Lewis acid promotes catalytic C-H bond hydroxylation with high chemo- and stereoselectivity. This reactivity pattern is observed with iron(II) complexes containing two cis-labile sites. The enhanced selectivity for C-H bond hydroxylation catalyzed by the high-spin iron(II) complexes in the presence of Sc3+ parallels that of the low-spin iron catalysts. Furthermore, the introduction of multimetal centers enhances the activity and selectivity of the iron catalyst. The study provides insights into the development of peroxide-dependent bioinspired catalysts for the selective oxygenation of C-H bonds without the restriction of using iron complexes of strong-field ligands.

Synthesis of poly(decahydro-2-naphthyl methacrylate)s with different geometric structures and effects of side-group dynamics on polymer properties investigated by thermal and dynamic mechanical analyses and DFT calculations

Ozaki, Anri,Sumita, Koha,Goto, Kunihiro,Matsumoto, Akikazu

, p. 2941 - 2950 (2013/06/05)

We prepared the geometric isomers of decahydro-2-naphthols as the source materials for the synthesis of poly(decahydro-2-naphthyl methacrylate)s [poly(DNMA)-I, -II, -III, and -IV] including alicyclic ester groups with different geometric structures. The geometry and conformational dynamics of the decahydro-2-naphthyl moieties were investigated by NMR spectroscopy and DFT calculations. We synthesized each isomer of the methacrylic monomers, polymerized them, and investigated the optical, thermal, and mechanical properties of poly(DNMA)s with different isomer compositions. The Tg values of the poly(DNMA)s were in the following order: 139.3 C for poly(DNMA)-II 3/g, 1.489, and 42-44, respectively.

Ytterbium triflate catalysed Meerwein-Ponndorf-Verley (MPV) reduction

Mollica, Adriano,Genovese, Salvatore,Pinnen, Francesco,Stefanucci, Azzurra,Curini, Massimo,Epifano, Francesco

experimental part, p. 890 - 892 (2012/03/08)

Ytterbium triflate was shown to be effective in promoting the reduction of substituted aromatic and aliphatic aldehydes and ketones using isopropanol as the solvent and the reducing agent. The whole process furnished the desired adducts in 22-98% yield.

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